K212790 · Biotec Italia, Srl · GEX · Aug 15, 2022 · General, Plastic Surgery
Device Facts
Record ID
K212790
Device Name
XLase Plus
Applicant
Biotec Italia, Srl
Product Code
GEX · General, Plastic Surgery
Decision Date
Aug 15, 2022
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 878.4810
Device Class
Class 2
Attributes
Therapeutic
Indications for Use
XLase Plus is indicated for use as follows: Diode 808/760 nm 4000W ALEX PRO Handpiece: Indicated for the treatment of hair removal with static and dynamic modes intended for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. · Treatment of Pseudofolliculitis barbae (PFB) · Use on all skin types (Fitzpatrick I-VI). SLP ND:YAG 1064 nm Handpiece: Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. (Skin Types Fitzpatrick I-V), photocoagulation and hemostasis of benign vascular lesions, treatment of benign pigmented lesions, such as but not limited to warts, telangiectasia, leg veins and spider veins. Q Switch ND:YAG 1064 nm Handpiece: Indicated for removal of dark tattoos and treatment of benign pigmented lesions. CPL Handpiece: Indicated for use Fitzpatrick skin types I – IV, as shown in the table below. Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. Photocoagulation of benign vascular lesions, photo thermolysis of blood vessels, treatment of benign pigmented lesions. ERBIUM:YAG FRACTIONAL 2940 nm Handpiece: Indicated for procedure requiring resurfacing of soft tissue with fractionated handpiece. Diode 2800W 810nm Handpiece: Indicated for use on all skin types I - VI), including tanned skin. Indicated for: - the treatment of benign vascular and benign pigmented lesions, - permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. Diode 1200W 810nm Handpiece: Indicated for use on all skin types (Fitzpatrick skin types I - VI), including tanned skin. Indicated for the treatment of benign vascular lesions, including angiomas, telangiectasia and other benign vascular lesions, and the treatment for pseudo folliculitis barbae. Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regime. Indicated for the treatment of benign pigmented lesions and leg veins. ALEX 755nm Handpiece: Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. Treatment of benign pigmented lesions. Treatment of wrinkles and the photocoagulation of dematological benign vascular lesions (such as port-wine stains, hemangiomas, telangiectasias). On all skin types (Fitzpatrick I-VI) including tanned skin.
Device Story
XLase Plus is a multi-module laser and pulsed light platform for dermatology and aesthetic surgery. Available in standing and tabletop configurations, it utilizes interchangeable handpieces (Diode, Nd:YAG, Erbium:YAG, CPL) to deliver energy for hair reduction, vascular/pigmented lesion treatment, tattoo removal, and skin resurfacing. The system consists of a console, touchscreen interface, and power supply. Operators (clinicians) select treatment parameters via the GUI; integrated safety functions restrict settings to predefined ranges. The device uses contact cooling (sapphire) for specific handpieces to enhance patient comfort. Energy delivery is triggered via foot or finger switch. By targeting specific chromophores (melanin, hemoglobin, water), the device achieves therapeutic effects like photothermolysis or tissue ablation. The system is intended for professional clinical use to provide stable, long-term hair reduction and dermatological lesion management.
Clinical Evidence
No clinical data was required to support substantial equivalence. Evidence consists of bench testing, including biocompatibility (ISO 10993-5, -10, -23), electrical safety/EMC compliance, and performance verification ensuring energy output remains within specified ranges.
Indicated for permanent hair reduction, treatment of Pseudofolliculitis barbae, benign vascular lesions (angiomas, hemangiomas, telangiectasias, leg/spider veins), benign pigmented lesions (warts), tattoo removal, and soft tissue resurfacing. Applicable to Fitzpatrick skin types I-VI depending on handpiece/wavelength. Prescription use only.
Regulatory Classification
Identification
(1) A carbon dioxide laser for use in general surgery and in dermatology is a laser device intended to cut, destroy, or remove tissue by light energy emitted by carbon dioxide.(2) An argon laser for use in dermatology is a laser device intended to destroy or coagulate tissue by light energy emitted by argon.
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August 15, 2022
Biotec Italia, SRL % Mike Berisha Offical Correspondent EVOSkin. LLC 6 Lincoln Knolll LN STE 100A Burlington, Massachusetts 01803
Re: K212790
Trade/Device Name: XLase Plus Regulation Number: 21 CFR 878.4810 Regulation Name: Laser surgical instrument for use in general and plastic surgery and in dermatology Regulatory Class: Class II Product Code: GEX, ONF Dated: July 11, 2022 Received: July 14, 2022
Dear Mike Berisha:
We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to legally marketed predicate devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general controls provisions of the Act. Although this letter refers to your product as a device, please be aware that some cleared products may instead be combination products. The 510(k) Premarket Notification Database located at https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm identifies combination product submissions. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. Please note: CDRH does not evaluate information related to contract liability warranties. We remind you, however, that device labeling must be truthful and not misleading.
If your device is classified (see above) into either class II (Special Controls) or class III (PMA), it may be subject to additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 898. In addition, FDA may publish further announcements concerning your device in the Federal Register.
Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal
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statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); medical device reporting of medical device-related adverse events) (21 CFR 803) for devices or postmarketing safety reporting (21 CFR 4, Subpart B) for combination products (see https://www.fda.gov/combination-products/guidance-regulatory-information/postmarketing-safety-reportingcombination-products); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820) for devices or current good manufacturing practices (21 CFR 4, Subpart A) for combination products; and, if applicable, the electronic product radiation control provisions (Sections 531-542 of the Act); 21 CFR 1000-1050.
Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR Part 807.97). For questions regarding the reporting of adverse events under the MDR regulation (21 CFR Part 803), please go to https://www.fda.gov/medical-device-safety/medical-device-reportingmdr-how-report-medical-device-problems.
For comprehensive regulatory information about mediation-emitting products, including information about labeling regulations, please see Device Advice (https://www.fda.gov/medicaldevices/device-advice-comprehensive-regulatory-assistance) and CDRH Learn (https://www.fda.gov/training-and-continuing-education/cdrh-learn). Additionally, you may contact the Division of Industry and Consumer Education (DICE) to ask a question about a specific regulatory topic. See the DICE website (https://www.fda.gov/medical-device-advice-comprehensive-regulatoryassistance/contact-us-division-industry-and-consumer-education-dice) for more information or contact DICE by email (DICE@fda.hhs.gov) or phone (1-800-638-2041 or 301-796-7100).
Sincerely,
Jianting Wang Acting Assistant Director DHT4A: Division of General Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Ouality Center for Devices and Radiological Health
Enclosure
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# Indications for Use
510(k) Number (if known) K212790
Device Name XLase Plus
Indications for Use (Describe) XLase Plus is indicated for use as follows:
Diode 808/760 nm 4000W ALEX PRO Handpiece: Indicated for the treatment of hair removal with static and dynamic modes intended for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime.
· Treatment of Pseudofolliculitis barbae (PFB)
· Use on all skin types (Fitzpatrick I-VI).
SLP ND:YAG 1064 nm Handpiece: Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. (Skin Types Fitzpatrick I-V), photocoagulation and hemostasis of benign vascular lesions, treatment of benign pigmented lesions, such as but not limited to warts, telangiectasia, leg veins and spider veins.
Q Switch ND:YAG 1064 nm Handpiece: Indicated for removal of dark tattoos and treatment of benign pigmented lesions.
CPL Handpiece: Indicated for use Fitzpatrick skin types I – IV, as shown in the table below. Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. Photocoagulation of benign vascular lesions, photo thermolysis of blood vessels, treatment of benign pigmented lesions.
| Pulsed light | Hair reduction | Benign | Blood vessels | Benign |
|------------------|------------------|------------------|------------------|-------------------|
| Wavelength range | | Vascular lesions | | Pigmented lesions |
| 500-1200nm | - | Skin Types I, II | Skin Types I, II | - |
| 520-1200nm | - | SkinType III | Skin Type III | Skin Types I, II |
| 550-1200nm | Skin Types I, II | - | - | Skin Type Ill |
| 595-1200nm | Skin Type III | - | - | - |
| 650-1200nm | Skin Type IV | - | - | Skin Type IV |
ERBIUM:YAG FRACTIONAL 2940 nm Handpiece: Indicated for procedure requiring resurfacing of soft tissue with fractionated handpiece.
Diode 2800W 810nm Handpiece: Indicated for use on all skin types I - VI), including tanned skin. Indicated for:
- the treatment of benign vascular and benign pigmented lesions,
- permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime.
Diode 1200W 810nm Handpiece:
Indicated for use on all skin types (Fitzpatrick skin types I - VI), including tanned skin.
Indicated for the treatment of benign vascular lesions, including angiomas, telangiectasia and other benign vascular lesions, and the treatment for pseudo folliculitis barbae.
Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regime.
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Indicated for the treatment of benign pigmented lesions and leg veins.
ALEX 755nm Handpiece: Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. Treatment of benign pigmented lesions. Treatment of wrinkles and the photocoagulation of dematological benign vascular lesions (such as port-wine stains, hemangiomas, telangiectasias). On all skin types (Fitzpatrick I-VI) including tanned skin.
Type of Use (Select one or both, as applicable)
| <div><span style="font-size:12px"><svg height="12" width="12"><rect fill="none" height="12" stroke="black" width="12"></rect><path d="M2,2 L10,10 M2,10 L10,2" stroke="black"></path></svg></span> Prescription Use (Part 21 CFR 801 Subpart D)</div> | <div><span style="font-size:12px"><svg height="12" width="12"><rect fill="none" height="12" stroke="black" width="12"></rect></svg></span> Over-The-Counter Use (21 CFR 801 Subpart C)</div> |
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Image /page/4/Picture/2 description: The image shows the logo for Biotec Italia. The logo features a stylized, abstract shape resembling a fingerprint or a topographical map, composed of several concentric lines. Below the graphic is the text "biotec Italia" in a lowercase, sans-serif font.
### 510(k) Summary
## This summary of 510(k) includes the safety and effectiveness information submitted in accordance with the requirements of 21 CFR 807.92
#### I. SUBMITTER BIOTEC ITALIA S. r. 1 Viale Della Repubblica 20 36031 Dueville VI, Italy
Email: info@biotecitalia.com Tel .: +39 0444 591683 Fax: +39 0444 361032
Establishment Registration Number: currently not registered.
#### SUBMISSION CORRESPONDENT and AUTHORIZED DISTRIBUTOR II.
Mike Berisha EVOSkin, LLC. 6 Lincoln Knoll Ln Ste 100A Burlington, MA 01803-4729
Establishment Registration Number: currently not registered. mike.berisha@evoskin.com Phone: 1 (786) 778-0419
#### III. DATE SUMMARY PREPARED: August 12, 2022
#### IV. SUBJECT DEVICE
Trade Name (proprietary name): XLase Plus Common or Usual Name: Medical Laser and Pulsed Light Platform Classification Name: Powered Laser Surgical Instrument Device Class: II Regulation Number: 21 CFR 878.4810 Product Code: GEX, ONF
#### V. PREDICATE DEVICE
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Section 6 - Page 2 of 17
XLase Plus Traditional 510(k) K212790
Image /page/5/Picture/2 description: The image shows a logo for "biotec Italia". The logo consists of a stylized, abstract shape resembling a fingerprint or a topographical map, composed of several concentric lines. Below the shape, the text "biotec Italia" is written in a lowercase, sans-serif font.
Trade Name: Deka Luxea 510k - K192539 El., EN. Electronic Engineering SPA Via Baldanzese 17 Calenzano, IT 50041
#### REFERENCE DEVICES VI.
Trade Name: Elysion Pro 510k - K193367
Trade Name: LightSheer Duet 510k - K053628
Trade Name: Dynamis Pro Family 510k - K143723
Trade Name: GentleMax Pro Plus 510k - K201111
#### VII. DEVICE DESCRIPTION
XLase Plus, laser for medical applications. It features two models: XLase Plus Standing (with wheels) and XLase Plus Table (tabletop).
The two medical devices are identical, contain the same electronic boards and the same critical components, use the same software and are able to perform the same aesthetic treatments. The generic components of XLase Plus Table are a subset of those of XLase Plus Standing. The difference between the two devices is that XLase Plus Standing is built on wheels while XLase Plus Table has no wheels but can be easily placed on a table due to its low weight. The device is for prescription use only.
The XLase Plus Standing and XLase Plus Table medical devices consists of:
- . System Console
- Operator control panel .
- . Touch screen monitor
- Power cable
- Accessories and components .
## Principles of Operation
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Image /page/6/Picture/1 description: The image shows the logo for Biotec Italia. The logo features a stylized, abstract shape resembling a fingerprint or a topographical map, composed of several concentric lines. Below the graphic is the text "biotec Italia" in a lowercase, sans-serif font.
The XLase Plus system principles of operation can be represented with the following block diagram:
## XLase Plus Standing and Table (Consoles) Principles of Operation / Mechanism of Action:
Image /page/6/Figure/5 description: The image shows a block diagram of an electronic system. The main power supply is 230 VAC, which is connected to a power supply of 24VDC. The 24VDC power supply is connected to a touchscreen display and a control board labeled BIO0912. The control board is also connected to a simmer board, and the main power supply and control board are connected to a driver, which is connected to capacitors, a diode handpiece, and a lamp handpiece.
### Proposed Conditions of Use
Temperature: 10 ℃ to 40 ℃ Relative humidity: 30% to 75%
### Technology
The XLase Plus offers the flexibility to perform different medical and aesthetic treatments due to different laser modules. Treatment parameters are set according to Indications for Use.
A range of values is available for each parameter. The integrated safety functions prevent the selection of values outside this range. However, because the settings of some parameters depend on other parameters, it is not always possible to use the full range of values for all parameters.
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Image /page/7/Picture/0 description: The image shows the logo for "biotec Italia". The logo consists of a stylized letter "b" formed by a series of concentric lines, creating a layered or topographic effect. Below the graphic is the text "biotec Italia" in a lowercase, sans-serif font.
| Spectrum and filter | |
|---------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Handpiece Type | Description |
| CPL | The wavelength range and filters determine the depth of light penetration and the spectral selectivity associated with the target chromophores. The 50x10mm optical guide determines the covered surface if the distal end of the optical guide is positioned perpendicular to the patient's skin. |
| Laser | SLP ND:YAG 1064 nm:<br>The size of the selected spacer determines the surface covered when the distal end of the tip is positioned perpendicular to the patient's skin. It will be chosen according to the characteristics of the vessel (diameter, depth).<br>ERBIUM:YAG FRACTIONAL 2940 nm:<br>The size of the selected spacer determines the covered surface of the treatment area that absorbs the laser energy when the distal end of the tip is positioned perpendicularly on the patient's skin.<br>QSWITCH ND: YAG 1064 nm:<br>The size of the selected spacer determines the surface covered when the distal end of the tip is positioned perpendicular to the patient's skin.<br>ALEX 755nm:<br>The size of the selected spacer determines the covered surface of the treatment area that absorbs the laser energy when the distal end of the tip is positioned perpendicular to the patient's skin |
| Diode handpiece* | Diode 808/760 nm 4000W ALEX PRO,<br>Diode 810nm 2800W and<br>Diode 810nm 1200W:<br>The 10x10mm optical guide determines the covered surface if the distal end of the optical guide is positioned perpendicular to the patient's skin. |
*CPL and Diode handpieces are equipped with an integrated cooling mechanism that provides continuous skin cooling through contact in the treatment area.
#### VIII. INDICATIONS FOR USE
XLase Plus is indicated for use as follows:
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Image /page/8/Picture/2 description: The image shows a logo for "biotec italia". The logo consists of a stylized, abstract shape resembling a fingerprint or a topographical map, composed of several concentric lines. Below the abstract shape, the text "biotec italia" is written in a lowercase, sans-serif font.
Diode 808/760 nm 4000W ALEX PRO Handpiece: Indicated for the treatment of hair removal with static and dynamic modes intended for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs regrowing when measured at 6, 9, and 12 months after the completion of a treatment regime.
· Treatment of Pseudofolliculitis barbae (PFB)
· Use on all skin types (Fitzpatrick I-VI).
SLP ND:YAG 1064 nm Handpiece: Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. (Skin Types Fitzpatrick I-VI), photocoagulation and hemostasis of benign pigmented and benign vascular lesions, treatment of benign pigmented lesions, such as but not limited to warts, telangiectasia, leg veins and spider veins.
Q Switch ND:YAG 1064 nm Handpiece: Indicated for removal of dark tattoos and treatment of benign pigmented lesions.
CPL Handpiece: Indicated for use Fitzpatrick skin types I - IV, as shown in the table below. Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. Photocoagulation of benign vascular lesions, photo thermolysis of blood vessels, treatment of benign pigmented lesions.
| Pulsed light | Hair reduction | Benign | Blood vessels | Benign |
|------------------|------------------|------------------|------------------|-------------------|
| Wavelength range | | Vascular lesions | | Pigmented lesions |
| 500-1200nm | - | Skin Types I, II | Skin Types I, II | - |
| 520-1200nm | - | Skin Type III | Skin Type III | Skin Types I, II |
| 550-1200nm | Skin Types I, II | - | - | Skin Type III |
| 595-1200nm | Skin Type III | - | - | - |
| 650-1200nm | Skin Type IV | - | - | Skin Type IV |
ERBIUM:YAG FRACTIONAL 2940 nm Handpiece: Indicated for procedure requiring resurfacing of soft tissue with fractionated handpiece.
Diode 2800W 810nm Handpiece: Indicated for use on all skin types (Fitzpatrick skin types I - VI), including tanned skin. Indicated for:
- the treatment of benign vascular and benign pigmented lesions,
- permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime.
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Image /page/9/Picture/1 description: The image shows a logo for "biotec Italia". The logo consists of a stylized shape resembling a fingerprint or a topographical map, formed by several concentric lines. Below the shape, the text "biotec Italia" is written in a lowercase, sans-serif font.
Diode 1200W 810nm Handpiece:
Indicated for use on all skin types (Fitzpatrick skin types I - VI), including tanned skin.
Indicated for the treatment of benign vascular lesions, including angiomas, hemangiomas, telangiectasia and other benign vascular lesions, and the treatment for pseudo folliculitis barbae.
Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime.
Indicated for the treatment of benign pigmented lesions and leg veins.
ALEX 755nm Handpiece: Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime. Treatment of benign pigmented lesions. Treatment of wrinkles and the photocoagulation of dermatological benign vascular lesions (such as port-wine stains, hemangiomas, telangiectasias). On all skin types (Fitzpatrick I- VI) including tanned skin.
#### COMPARISON OF TECHNOLOGICAL CHARACTERISTICS WITH THE IX. PREDICATE AND REFERENCE DEVICES
| | Subject Device<br>XLase Plus | Predicate Device<br>Deka Luxea<br>K192539 | Reference Device<br>Elysion Pro<br>K193367 | Reference Device<br>LightSheer Duet<br>K053628 | Reference Device<br>Dynamis Pro Family<br>K143723 | Reference Device<br>GentleMax Pro Plus<br>K201111 | | Storage<br>Conditions | Sterilization | Packaging | Body areas of<br>application | Duration of Body<br>Contact | User Interface | Software | The human machine interface was developed with "Touch Win Edit Tool"<br>The processor used is by ARM7 LCD MCU Display is a 208-LQFP - LPC2470FBD208 from semiconductor manufacturer NXP. | Unknown type | Unknown type | Unknown type | Unknown type | Unknown type | Pulse Repetition Rate<br>(Hz): 1-8 Hz ± 20 %<br>(0.8-10.0 Hz) | | Pulse Repetition Rate<br>(Hz): Static up to 3Hz<br>Dynamic 5-15 Hz | | | |
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| Medical Device<br>Common Name | Medical Laser and<br>Pulsed Light platform | Medical Laser and<br>pulsed Light platform | Diode Laser Hair<br>Removal System | Pulsed Diode Array<br>Laser | Er:YAG/Nd:YAG<br>Surgical Laser | Dermatology Laser<br>System | | Temperature (-10 - 38<br>℃) or (-14 to 100 ℉).<br>Relative humidity %<br>range is 1.5% to 90%. | N/A | A wooden pallet: this<br>pallet (80 x 65 x 11<br>cm for Table and 82 x<br>76 x 64 cm for ) is<br>made of wood treated<br>according to ISPM-15<br>- Cardboard box on<br>the outside;<br>- Polyurethane foam<br>- Transportation<br>monitoring:<br>Shockwave label<br>Tiltwatch label<br>Data logger<br>(temperature and<br>humidity) | Feet, Legs, Hip,<br>Thigh, Abdomen,<br>Chest, Shoulders,<br>Back, Arms, Neck,<br>Face and Hands | The material with<br>direct tissue contact<br>with the skin is the<br>stainless steel from<br>(spacers, and diode<br>handpieces) with<br>contact duration (A)<br>for ≤ 24 hours. | Display screen<br>(software XLASE<br>PLUS) | | | | Handpieces | | | | (Long Pulse or Static<br>up) to 3 Hz<br>(Motion Speed or<br>Dynamic) up to 5-10<br>Hz | | | | | |
| Manufacturer: | BIOTEC ITALIA<br>S.R.L. | DEKA M.E.L.A. | High Technology<br>Products, S.L.U | LUMENIS LTD. | FOTONA | CANDELA<br>CORPORATION | | Temperature: 5 ℃ to<br>50 ℃<br>Relative humidity:<br>30% to 95% | N/A | Unknown | Feet, Legs, Hip, Thigh,<br>Abdomen, Chest,<br>Shoulders, Back,<br>Arms, Neck, Face and<br>Hands. | Contact duration (A)<br>for ≤ 24 hours. | The Touch<br>Screen/Display Panel<br>provides a simple<br>graphical user<br>interface (GUI) from<br>which you can set the<br>operating mode, laser<br>parameters DCD | | Indications for Use | | | | | | Cooling Temperature:<br>(Sapphire cooling) 5°C | | Cooling Temperature:<br>(Sapphire cooling) 5°C | | | |
| Console | XLase Plus Standing<br>and Table | Deka Luxea | Elysion Pro | LightSheer Duet | Dynamis Pro | GentleMax Pro | | Temperature: 2 - 50<br>℃<br>Relative humidity<br><90% (without<br>condensation) | N/A | Unknown | Feet, Legs, Hip, Thigh.<br>Abdomen, Chest,<br>Shoulders, Back, Arms.<br>Neck, Face and Hands. | Contact duration (A)<br>for ≤ 24 hours. | The console provides<br>touchscreen computer<br>control | Diode 808/760 nm 4000W ALEX PRO Handpiece | Diode 808/760 nm 4000W ALEX PRO:<br>Indicated for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime.<br>• Treatment of Pseudofolliculitis barbae (PFB)<br>• Use on all skin types (Fitzpatrick I-VI). | | Elysion handpiece:<br>Indications for use for ELYSION diode laser hair removal system with 755nm and 810nm applicators include:<br>• Hair Removal with Static and Dynamic modes intended for permanent reduction in hair regrowth, defined as a long term, stable reduction in the number of hairs re-growing when measured at 6, 9, and 12 months after the completion of a treatment regime.<br>• Treatment of Pseudofolliculitis barbae (PFB)<br>• Use on all skin types (Fitzpatrick I-VI). | | | | | Indications for Use | | | | |
| Product Code | GEX, ONF | GEX, ONF | GEX | GEX | GEX, ONG | GEX | | Temperature: -5℃ -<br>55℃ 23℉ - 131℉<br>Relative humidity:<br>90% @ 35℃, 32% @<br>55℃ | N/A | Unknown | Feet, Legs, Hip, Thigh,<br>Abdomen, Chest,<br>Shoulders, Back, Arms,<br>Neck, Face and Hands. | Contact duration (A)<br>for ≤ 24 hours. | The console provides<br>touchscreen computer<br>control | | Specifications | | | | | | Laser SLP<br>ND:YAG<br>1064nm<br>Handpiece | SLP ND:YAG 1064<br>nm Handpiece:<br>Indicated for<br>permanent reduction in<br>hair regrowth, defined<br>as a long term, stable<br>reduction in the<br>number of hairs re-<br>growing when<br>measured at 6, 9, and<br>12 months after the<br>completion of a<br>treatment regime.<br>(Skin Types<br>Fitzpatrick I-VI),<br>photocoagulation and<br>hemostasis of benign<br>pigmented and benign<br>vascular lesions,<br>treatment of benign<br>pigmented lesions,<br>such as but not limited<br>to warts,<br>telangiectasia, leg<br>veins and spider veins. | SPARKS LASER<br>handpiece:<br>Indicated for removal<br>of unwanted hair, for<br>stable long term or<br>permanent hair<br>reduction (Skin Types<br>Fitzpatrick I-VI),<br>photocoagulation and<br>hemostasis of benign<br>pigmented and<br>vascular lesions, such<br>as but not limited to<br>warts,<br>telangiectasia, leg<br>veins and spider veins,<br>treatment of benign<br>pigmented lesions. | | | |
| Configuration | •System Console<br>•Operator control<br>panel<br>•Touch screen monitor<br>•Laser handpiece(s)<br>•Diode(s) handpiece(s) | •System Console<br>•Operator control<br>panel<br>•Touch screen monitor<br>•Laser handpiece(s)<br>•Diode(s) handpiece(s) | •System Console<br>•Operator control panel<br>•Touch screen monitor<br>•Diode handpiece | •System Console<br>•Operator control<br>panel<br>•Touch screen<br>monitor<br>•Laser handpiece(s)<br>•Diode(s)<br>handpiece(s) | •System Console<br>•Operator control panel<br>•Touch screen monitor<br>•Laser handpiece(s)<br>•Diode(s) handpiece(s) | •System Console<br>•Operator control<br>panel<br>•Touch screen<br>monitor<br>•Laser handpiece(s)<br>•Diode(s)<br>handpiece(s) | | Relative humidity:<br>30% to 75% -non<br>condensing<br>Temperature: -40 ℃ to<br>+70 ℃ (without<br>cooling water)<br>Relative humidity: 10%<br>to 100% condensing | N/A | Unknown | Feet, Legs, Hip, Thigh,<br>Abdomen, Chest,<br>Shoulders, Back, Arms,<br>Neck, Face and Hands. | Contact duration (A) for<br>≤ 24 hours. | Touch screen | | Product Code: GEX | | Product Code: GEX | | | | | Specifications | | | | |
| Emission<br>Activation | Foot or finger switch | Foot or finger switch | Finger switch | Foot or finger switch | Foot or finger switch | Foot or finger switch | | Temperature:<br>40℉ and 110℉ F (4.5℃<br>and 43℃).<br>Relative humidity:<br>30% to 95% | N/A | Unknown | Feet, Legs, Hip,<br>Thigh, Abdomen,<br>Chest, Shoulders,<br>Back, Arms, Neck,<br>Face and Hands. | Contact duration (A)<br>for ≤ 24 hours. | The Touch<br>Screen/Display Panel<br>provides a simple<br>graphical user<br>interface (GUI) from<br>which you can set the<br>operating mode, laser<br>parameters DCD<br>parameters | | Laser Wavelength:<br>808, 760 nm | | Laser Wavelength: 810 nm, 755 nm | | | | | Product Code: GEX | Product Code: GEX | | | |
| Electrical<br>specifications | 115-240v ~, 50-60Hz,<br>2300VA max. | 115-240v ~, 50-60Hz,<br>2300VA max. | 115-240v ~, 50-60Hz,<br>2300VA max. | 115-240v ~, 50-60Hz,<br>2300VA max. | 115-240v ~, 50-60Hz,<br>2300VA max. | 115-240v ~, 50-60Hz,<br>2300VA max. | Fluence: 32 J/cm2 ± 20 % (24 - 40 J/cm2) | | Fluence: 40 J\cm² | | | | | | Laser Wavelength:<br>1064 nm | Laser Wavelength:<br>1064 nm | | | | | | | | | | |
| Operating<br>Environment | Temperature: 10 °C to<br>40 °C Relative<br>humidity: 30% to 75% | Temperature: 10 °C to<br>40 °C Relative<br>humidity: 30% to 75% | Temperature: 18 °C<br>to 28 °C | Temperature: 10 °C to<br>40 °C<br>Relative humidity: 30%<br>to 75% | Temperature:<br>ambient temperature<br>range +10 °C to<br>+25 °C; | Temperature:<br>65° and 85°F (18° and<br>29°C).<br>Relative humidity:<br>30% to 75% | | Handpiece Spot Size:<br>Spot Size 15 mm - 15 x 10mm ± 20 % (12-18 x 8-12 mm)<br>Spot Size 9 mm - 9 x 9 mm ± 20 % (7.2-10.8 x 7.2-10.8 mm) | | Handpiece Spot Size:<br>10 x 10, 18 x 10mm | | | | | Fluence:<br>(2.5 mm) 100-584 ±<br>20 % J/cm² (80 - 700<br>J/cm²)<br>(4<br>mm) 30-250 ± 20 %<br>J/cm² (24 - 300<br>J/cm²)<br>(6 mm) - 50 - 136<br>J/cm² ± 20 % (40 -<br>170 J/cm²)<br>(10 mm) 4 - 48 ± 20<br>% J/cm²<br>(5 - 60 J/cm²) | Fluence:<br>80-700 J/cm² (2.5<br>mm)<br>30 -250 J/cm² (4 mm)<br>14-170 J/cm² (6 mm)<br>5-60 J/cm² (10 mm) | | | | | | | | | | |
| | Pulse Duration: up to 120 ms<br>Min Pulse Duration: 10 ms ± 20 % (8 - 12 ms)<br>Max Pulse Duration 100 ms ± 20 % (80-120 ms) | | Pulse Duration: 3 - 400 ms | | | | | Spot Size (2.5 mm) -<br>2.5 mm ± 20 % (2 - 3 mm) | Handpiece Spot Sizes:<br>Ø 2.5, 4, 6, 10 mm | | | | | | | | | | | | | | | | | |
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Image /page/10/Picture/0 description: The image shows the logo for "biotec Italia". The logo consists of a stylized, abstract shape resembling a fingerprint or a topographical map, composed of several concentric lines. Below the shape, the text "biotec Italia" is written in a lowercase, sans-serif font.
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Image /page/11/Picture/0 description: The image shows the logo for Biotec Italia. The logo features a stylized, abstract shape resembling a fingerprint or a topographical map, composed of several concentric lines. Below the graphic is the text "biotec italia" in a lowercase, sans-serif font.
Section 6 - Page 8 of 17
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Image /page/12/Picture/0 description: The image shows the logo for Biotec Italia. The logo features a stylized, abstract shape resembling a fingerprint or a topographical map, composed of several concentric lines. Below the graphic is the text "biotec italia" in a lowercase, sans-serif font.
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Image /page/13/Picture/4 description: The image shows the logo for Biotec Italia. The logo features a stylized letter "b" formed by a series of concentric, rounded shapes, resembling contour lines on a map. Below the symbol, the words "biotec Italia" are written in a lowercase, sans-serif font.
Section 6 - Page 10 of 17
| | Spot Size (4 mm) - 4<br>mm ± 20 % (3.2 -<br>4.8mm)<br>Spot Size (6 mm) - 6<br>mm ± 20 % (4.8 - 7.2<br>mm)<br>Spot Size (10 mm) -<br>10 mm ± 20 % (8 -<br>12mm) | | | | |
|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------|--|
| | Pulse Duration:<br>Min Pulse Duration -<br>250 us ± 20 %<br>(200 - 300 us) = 0.25<br>ms ± 20 % (0.20 –<br>0.30 ms)<br>Max Pulse Duration<br>50 ms ± 20 %<br>(40 - 60 ms) = 50000<br>us ± 20 % (40000 -<br>60000 us) | Pulse Duration: 1 -<br>280 ms | | | |
| | Pulse Repetition Rate:<br>1 - 8 Hz ± 20 %<br>(0.8 - 10.0 Hz) | Pulse Repetition<br>Rate:<br>Single shot to 10 Hz | | | |
| | | Indications for Use | | | |
| | Laser QS ND:YAG<br>1064 nm:<br>Indicated for removal<br>of dark tattoos and<br>treatment of benign<br>pigmented lesions. | PRISMA LASER<br>handpiece:<br>Indicated for removal<br>of dark tattoos and<br>treatment of benign<br>pigmented lesions. | | | |
| | Specifications | | | | |
| | Product Code: GEX<br>Laser Wavelength:<br>1064 nm | Product Code: GEX<br>Laser Wavelength:<br>1064 nm | | | |
| Laser QS ND:YAG<br>1064 nm<br>Handpiece | Fluence:<br>(2.5 mm) - 17 J/cm2 ±<br>20 % (13.6 - 20.4<br>J/cm2) | Fluence: 14 J/cm2 (2.5<br>x 2.5 mm),<br>9<br>J/cm2 (3 x 3 mm) | | | |
| | Handpiece Spot Size:<br>Spot Size (2.5 mm) -<br>2.5 mm ± 20 % (2 -<br>3mm) | Handpiece Spot Sizes:<br>2.5 x 2.5 mm, 3 x 3<br>mm | | | |
|…
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Learn the FDA Browser
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.