BEGO Semados® Trays are intended to store and organize the BEGO Semados® medical devices during both steam sterilization in an autoclave and implant/ prosthetic treatments. BEGO Semados® Trays are not intended on their own to maintain sterility; they are intended to be used with a legally marketed, validated, FDA-cleared sterilization pouch.
Device Story
BEGO Semados® Trays (models 58350, 58349, 58356, 58357) serve as organizational containers for surgical and prosthetic instruments; used in healthcare facilities during steam sterilization and clinical procedures. Trays feature perforated designs for steam penetration; some models include silicone grommets to secure instruments. Trays are not sterile barriers; must be used with FDA-cleared sterilization pouches. Healthcare providers use trays to organize workflows; instruments are placed in designated slots/holes. Benefits include standardized instrument organization and validated sterilization compatibility. Trays are reusable and processed via fractionated pre-vacuum steam sterilization (132°C, 4 min exposure, 20 min drying).
Clinical Evidence
Bench testing only. Validations included automated cleaning (protein/TOC analysis per AAMI TIR30), cytotoxicity (ISO 10993-5), sterilization validation (ISO 17665-1/ANSI/AAMI ST77) achieving SAL 10^-6, and drying time testing (AAMI TIR12).
Technological Characteristics
Materials: Polyphenylsulfone (PPSU Radel® R5000), Polypropylene (PP-HS), and silicone rubber. Perforated design for steam penetration. Dimensions range from 80x85x28mm to 188.1x138.7x61.5mm. Sterilization: Fractionated pre-vacuum steam (132°C).
Indications for Use
Indicated for storage and organization of BEGO Semados® surgical instruments, insertion tools, drill stops, and prosthetic instruments during steam sterilization and clinical procedures. Not intended to maintain sterility independently; requires use with a validated, FDA-cleared sterilization pouch.
Regulatory Classification
Identification
A sterilization wrap (pack, sterilization wrapper, bag, or accessories, is a device intended to be used to enclose another medical device that is to be sterilized by a health care provider. It is intended to allow sterilization of the enclosed medical device and also to maintain sterility of the enclosed device until used.
{0}------------------------------------------------
Image /page/0/Picture/0 description: The image shows the logo of the U.S. Food and Drug Administration (FDA). The logo consists of two parts: the Department of Health & Human Services logo on the left and the FDA logo on the right. The FDA logo is a blue square with the letters "FDA" in white, followed by the words "U.S. FOOD & DRUG ADMINISTRATION" in blue.
February 18, 2021
BEGO Implant Systems GmbH & Co. KG Bertrand Lecointe Regulatory Affairs Manager Wilhelm-Herbst-Str. 1 Bremen, 28359 De
Re: K201412
Trade/Device Name: BEGO SEMADOS Tr 58350, BEGO Semados Tr 58349, BEGO Semados DSTr 58356, BEGO SEMADOS PKTr 58357 Regulation Number: 21 CFR 880.6850 Regulation Name: Sterilization Wrap Regulatory Class: Class II Product Code: KCT Dated: January 19, 2021 Received: January 25, 2021
Dear Bertrand Lecointe:
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 statutes and regulations administered by other Federal agencies. You must comply with all the Act's
{1}------------------------------------------------
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 (OS) 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,
Clarence Murray III, Ph.D. Acting Assistant Director DHT4B: Division of Infection Control and Plastic Surgery Devices OHT4: Office of Surgical and Infection Control Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
{2}------------------------------------------------
# Indications for Use
510(k) Number (if known)
#### Device Name
BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados® DSTr 58356, BEGO SEMADOS® PKTr 58357
Indications for Use (Describe)
{3}------------------------------------------------
| Type of Use (Select one or both, as applicable) | |
|-------------------------------------------------|--|
|-------------------------------------------------|--|
| Prescription Use (Part 21 CFR 801 Subpart D)
X Over-The-Counter Use (21 CFR 801 Subpart C)
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# 510(k) Summary K201412
| Submitter Information: | BEGO Implant Systems GmbH & Co. KG<br>Wilhelm-Herbst-Str. 1<br>28359 Bremen, Germany<br>Phone: +49 (0) 421 2028-246<br>Fax: +49 (0) 421 2028-265<br>Establishment Registration Number: 3008252251<br>Owner/Operator Number: 10028/893 |
|----------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| Official Correspondent: | Kathleen Al-Kaissy, Regulatory Affairs Manager<br>BEGO Implant Systems GmbH & Co. KG<br>Phone: +49 (0) 421 2028-338<br>E-Mail: IM-RA@bego.com |
| Application Correspondent: | Bertrand Lecointe, Regulatory Affairs Manager<br>BEGO Implant Systems GmbH & Co. KG<br>Phone: +49 (0) 421 2028-230<br>E-Mail: IM-RA@bego.com |
| Date Prepared: | 2/17/2021 |
| 510(k) No.: | K201412 |
| Name of Device: | BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Se-<br>mados® DSTr 58356, BEGO SEMADOS® PKTr 58357 |
| Common name: | BEGO Semados® Trays |
| Classification Name: | Sterilization Wrap Containers, Trays, Cassettes & Other Accessories |
| Product Code: | KCT |
| C.F.R. Section: | 21 CFR 880.6850 |
| Classification Panel: | General Hospital |
| Regulation Class: | Class II |
# Predicate Device Information
# Primary Predicate
| Device Trade Name: | Straumann BLX Surgical Cassette |
|--------------------|---------------------------------|
| Applicant: | Institut Straumann AG |
| 510(k) No.: | K180791 |
| Reference Device | |
| Device Trade Name: | PureSet Tray |
| Applicant: | Nobel Biocare AB |
| 510(k) No.: | K181075 |
{5}------------------------------------------------
# Device(s) Identification
Subject of this submission are the BEGO Semados® Trays (58350, 58349, 58356, 58357) that are parts of BEGO Semados® implant/ prosthetic treatment sets/ kits. The below table specifies the devices that are subject of this submission. The empty trays are highlighted in bold in all tables of this submission for identification purposes.
| | Trade or Proprietary or Model Name for This Device | Model<br>number | Product Code |
|---|----------------------------------------------------|-----------------|------------------------------|
| 1 | BEGO SEMADOS® Tr 58350 | 58350 | KCT |
| | BEGO SEMADOS® RS/RSX-LINE TRAY PLUS | 57949 | Kit containing<br>device KCT |
| 2 | BEGO Semados® Tr 58349 | 58349 | KCT |
| | BEGO Semados® Tr 58348 | 58348 | Kit containing<br>device KCT |
| 3 | BEGO Semados® DSTr 58356 | 58356 | KCT |
| | DRILL STOP TRAY PLUS (RS/RSX-LINE) | 57483 | Kit containing<br>device KCT |
| 4 | BEGO SEMADOS® PKTr 58357 | 58357 | KCT |
| | PROSTHETIC KIT | 55826 | Kit containing<br>device KCT |
#### Overview BEGO Semados® Trays
Note: The instruments and accessory devices that are intended to be sterilized and stored in the subject Trays, are not subject to this submission.
{6}------------------------------------------------
### Indications for use
BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados® DSTr 58356, BEGO SEMA-DOS® PKTr 58357 are intended to store and organize the BEGO Semados® surgical instruments, insertion tools, drill stops and prosthetic instruments during both steam sterilization in an autoclave and implant/ prosthetic treatments.
BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados® DSTr 58356, BEGO SEMA-DOS® PKTr 58357 are not intended on its own to maintain sterility; it is intended to be used with a legally marketed, validated, FDA-cleared sterilization pouch.
| Cycle | Temperature | Exposure Time | Drying Time |
|--------------------------------|---------------|---------------|-------------|
| Fractioned pre-vacuum<br>steam | 132°C (270°F) | 4 min | 20 min |
Sterilization validations included the worst-case load configurations and has the maximum load including instruments for the following device models:
| Device Model | Maximum load (wt),<br>including instruments | Type of Instruments |
|--------------------------|---------------------------------------------|-----------------------------------------|
| BEGO SEMADOS® Tr 58350 | 476 g | Surgical instruments, insertion tools |
| BEGO Semados® Tr 58349 | 261 g | Surgical instruments, insertion tools |
| BEGO Semados® DSTr 58356 | 137 g | Drill stops |
| BEGO SEMADOS® PKTr 58357 | 220 g | Insertion tools, prosthetic instruments |
Healthcare facilities should not exceed 25 pounds (BEGO Semados® Trays containment device + sterile pouch + surgical instruments/insertion tools/drill stop/prosthetic instruments).
Sterilization validations included the worst-case load configurations of following lumen sizes and dimensions and has the maximum load for the following device models:
| Device Model | Type of Lumen | Number of lumens | Sizes & Dimensions [mm] |
|--------------------------|---------------|------------------|-----------------------------------------------------------------|
| BEGO SEMADOS® Tr 58350 | Drill holes | 8 | Ø1.2, L2.4 / Ø 1.2, L 6.8 / Ø 2.4-2.9, L 22.5/14.6 / Ø1.2, L6.8 |
| | Oval hole | 1 | 2.3 x 2.0 |
| BEGO Semados® Tr 58349 | Drill holes | 4 | Ø1.2, L2.4 / Ø2.4, L16 |
| | Oval hole | 1 | 2.3x2.0 |
| BEGO Semados® DSTr 58356 | Drill holes | 25 | Ø 2.6-5.1, L 6-12 |
| BEGO SEMADOS® PKTr 58357 | Drill holes | 5 | Ø 2.4, L16 / Ø 1.2, L 6.8 |
BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados® DSTr 58356, BEGO SEMA-DOS® PKTr 58357 are offered in the following sizes:
| Device Model | Dimensions [mm] |
|--------------------------|----------------------|
| BEGO SEMADOS® Tr 58350 | 188.1 x 138.7 x 61.5 |
| BEGO Semados® Tr 58349 | 142.7 x 99.6 x 61 |
| BEGO Semados® DSTr 58356 | 80 x 85 x 28 |
| BEGO SEMADOS® PKTr 58357 | 140 x 80 x 25 |
{7}------------------------------------------------
### Device Description
#### BEGO SEMADOS® Tr 58350
BEGO SEMADOS® Tr 58350 is composed of three main components: a tray cover, a tray container and a tray insert, all made of polyphenylsulfone. The tray container and the tray insert have additional silicone rubber grommets to store and organize the BEGO Semados® surgical instruments and insertion tools. The tray container and tray insert are printed to indicate the surgical workflow and the position of the above mentioned instruments within the tray for reprocessing and implant/ prosthetic treatments.
BEGO SEMADOS® Tr 58350 is supplied without BEGO Semados® surgical instruments and insertion tools.
BEGO SEMADOS® RS/RSX-LINE TRAY PLUS is supplied as a kit with BEGO SEMADOS® Tr 58350 and BEGO Semados® surgical instruments and insertion tools.
#### BEGO Semados® Tr 58349
BEGO Semados® Tr 58349 is composed of three main components: a tray cover, a tray container and a tray insert, all made of polyphenylsulfone. The tray container and the tray insert have additional silicone rubber grommets to store and organize the BEGO Semados® surgical instruments and insertion tools. The tray container and tray insert are printed to indicate the surgical workflow and the position of the above mentioned instruments within the tray for reprocessing and implant/ prosthetic treatments.
BEGO Semados® Tr 58349 is supplied without BEGO Semados® surgical instruments and insertion tools.
BEGO Semados® Tr 58348 is supplied as a kit with BEGO Semados® Tr 58349 and BEGO Semados® surgical instruments and insertion tools.
#### BEGO Semados® DSTr 58356
BEGO Semados® DSTr 58356 is composed of two main components: a tray cover made of polyphenylsulfone and a tray container made of polypropylene. The tray container has inserts to store and organize the drill stops. The tray container is printed to indicate the position of the drill stops within the tray for reprocessing and implant treatments.
BEGO Semados® DSTr 58356 is supplied without drill stops.
DRILL STOP TRAY PLUS (RS/RSX-Line) is supplied as a kit with BEGO Semados® DSTr 58356 and drill stops.
#### BEGO SEMADOS® PKTr 58357
BEGO SEMADOS® PKTr 58357 is composed of two main components: a tray cover made of polyphenylsulfone and a tray container made of polypropylene. The tray container has inserts to store
{8}------------------------------------------------
and organize the BEGO Semados® insertion tools and prosthetic instruments. The tray container is printed to indicate the position of the above mentioned instruments within the tray for reprocessing and implant/prosthetic treatments.
BEGO SEMADOS® PKTr 58357 is supplied without BEGO Semados® insertion tools and prosthetic instruments.
PROSTHETIC KIT is supplied as a kit with BEGO SEMADOS® PKTr 58357 and BEGO Semados® insertion tools and prosthetic instruments.
#### Intended Use:
BEGO Semados® Trays are intended to store and organize the BEGO Semados® medical devices during both steam sterilization in an autoclave and implant/ prosthetic treatments.
BEGO Semados® Trays are not intended on their own to maintain sterility; they are intended to be used with a legally marketed, validated, FDA-cleared sterilization pouch.
{9}------------------------------------------------
## Summary of technological characteristics
The below table presents the comparison of functions and parameters of the identified Predicate Device and the BEGO Semados® Trays.
#### Subject Device Predicate Device Feature BEGO Semados® Trays (K201412) Straumann BLX Surgical Cassette Comparison (K180791) BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados® The Straumann BLX Cassette is used in DSTr 58356, BEGO SEMADOS® PKTr 58357 are intended to store and healthcare facilities to organize, enclose, sterorganize the BEGO Semados® surgical instruments, insertion tools, ilize, transport, and store medical devices bedrill stops and prosthetic instruments during both steam sterilizatween surgical uses. The BLX Cassette is not tion in an autoclave and implant/ prosthetic treatments. intended to maintain sterility; it is intended to BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados® conjunction with a legally marketed, validated DSTr 58356, BEGO SEMADOS® PKTr 58357 are not intended on its own sterilization wrap. to maintain sterility; it is intended to be used with a legally mar-The BLX Cassette has been validated for a keted, validated, FDA-cleared sterilization pouch. maximum load of 300 grams, including cas-Cycle Temperature Exposure Drying sette and instruments. Time Time Fractioned pre-132°C (270°F) 4 min 20 min Sterilization parameters: Pre-vacuum steam: Indications for Use vacuum steam Similar 132°C (270°F) for 4 minutes with 20 minutes drying time. Sterilization validations included the worst-case load configurations and has the maximum load including instruments for the following device models: Device Model Maximum load Type of Instruments (wt), including instruments BEGO SEMADOS® Tr Surgical instruments, in-476 g 58350 sertion tools BEGO Semados® Tr Surgical instruments, in-261 g 58349 sertion tools BEGO Semados® 137 g Drill stops DSTr 58356
#### Comparison between Subject and Predicate Device
{10}------------------------------------------------
| | Subject Device | | | | Predicate Device | |
|---------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------|-------------------------|------------------------------------------------------------------------------------|----------------------------------------------|------------|
| Feature | BEGO Semados® Trays (K201412) | | | | Straumann BLX Surgical Cassette<br>(K180791) | Comparison |
| | BEGO SEMADOS®<br>PKTr 58357 | 220 g | | Insertion tools, pros-<br>thetic instruments | | |
| | Healthcare facilities should not exceed 25 pounds (BEGO Semados®<br>Trays containment device + sterile pouch + surgical instruments/inser-<br>tion tools/drill stop/prosthetic instruments). | | | | | |
| | Sterilization validations included the worst-case load configurations of<br>following lumen sizes and dimensions and has the maximum load for<br>the following device models: | | | | | |
| | Device Model | Type of<br>Lumen | Number<br>of lu-<br>men | Sizes & Dimensions<br>[mm] | | |
| BEGO SEMADOS®<br>Tr 58350 | | Drill holes | 8 | $Ø$ 1.2, L2.4 / $Ø$ 1.2,<br>L 6.8 / $Ø$ 2.4-2.9,<br>L 22.5/14.6 / $Ø$ 1.2,<br>L6.8 | | |
| | | Oval hole | 1 | 2.3 x 2.0 | | |
| | BEGO Semados® | Drill holes | 4 | $Ø$ 1.2, L2.4 / $Ø$ 2.4, L16 | | |
| | Tr 58349 | Oval hole | 1 | 2.3x2.0 | | |
| | BEGO Semados®<br>DSTr 58356 | Drill holes | 25 | $Ø$ 2.6-5.1, L 6-12 | | |
| | BEGO SEMADOS®<br>PKTr 58357 | Drill holes | 5 | $Ø$ 2.4, L16 / $Ø$ 1.2, L<br>6.8 | | |
| | BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados®<br>DSTr 58356, BEGO SEMADOS® PKTr 58357 are offered in the following<br>sizes: | | | | | |
| | Device Model | | | Dimensions [mm] | | |
| | BEGO SEMADOS® Tr 58350 | | | 188.1 x 138.7 x 61.5 | | |
| | BEGO Semados® Tr 58349 | | | 142.7 x 99.6 x 61 | | |
| | BEGO Semados® DSTr 58356 | | | 80 x 85 x 28 | | |
| | BEGO SEMADOS® PKTr 58357 | | | 140 x 80 x 25 | | |
{11}------------------------------------------------
| | | Subject Device | Predicate Device | |
|---------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------|
| Feature | | BEGO Semados® Trays (K201412) | Straumann BLX Surgical Cassette<br>(K180791) | Comparison |
| Intended Use | | BEGO Semados® Trays are intended to store and organize the BEGO<br>Semados® medical devices during both steam sterilization in an au-<br>toclave and implant/ prosthetic treatments.<br>BEGO Semados® Trays are not intended on their own to maintain<br>sterility; they are intended to be used with a legally marketed, vali-<br>dated, FDA-cleared sterilization pouch. | The Straumann BLX Cassette is used in<br>healthcare facilities to organize, enclose, ster-<br>ilize, transport, and store medical devices be-<br>tween surgical uses. The BLX Cassette is not<br>intended to maintain sterility; it is intended to<br>conjunction with a legally marketed, validated<br>sterilization wrap. | Identical |
| Product Code | | KCT | KCT | Identical |
| Reusable | | Yes | Yes | Identical |
| Sterilization<br>Method | | Moist Heat (Steam) | Moist Heat (Steam) | Identical |
| Cycle | | Dynamic-Air-Removal (fractionated vacuum) | Pre-vacuum | Identical |
| Temperature | | 132°C (270°F) | 132°C (270°F) | Identical |
| Exposure time | | 4 minutes | 4 minutes | Identical |
| Drying time | | 20-30 minutes | 20 minutes | Similar |
| Sterile Barrier | | FDA-cleared sterilization pouch | FDA-cleared sterilization wrap | Different |
| Maximum Load | Device Model | Maximum load (wt), including instruments | 300g, including cassette and instruments | Different |
| | BEGO SEMADOS® Tr 58350 | 476 g | | |
| | BEGO Semados® Tr 58349 | 261 g | | |
| | BEGO Semados® DSTr 58356<br>BEGO SEMADOS® PKTr 58357 | 137 g<br>220 g | | |
| Vent to volume ratio | Device Model | V-to-V ratio | 0.054 in 2/in3 | Different |
| | BEGO SEMADOS® Tr 58350 | 0.084 in2/in3 | | |
| | Subject Device | Predicate Device | | |
| Feature | BEGO Semados® Trays (K201412) | Straumann BLX Surgical Cassette (K180791) | Comparison | |
| | BEGO Semados® Tr 58349 0.072 in²/in³<br>BEGO Semados® DSTr 58356 0.601 in²/in³<br>BEGO SEMADOS® PKTr 58357 0.241 in²/in³ | | | |
| Device Construction | BEGO SEMADOS® Tr 58350/ BEGO Semados® Tr 58349:<br>Plastic tray, lid and insert<br>BEGO Semados® DSTr 58356/<br>BEGO SEMADOS® PKTr 58357:<br>Plastic tray and lid | Plastic tray and lid | Similar | |
| Perforated | Yes, allows moist heat (steam) penetration to achieve sterilization | Yes, allows moist heat (steam) penetration to achieve sterilization | Identical | |
| Material Composition | BEGO SEMADOS® Tr 58350/ BEGO Semados® Tr 58349:<br>- Polyphenylsulfone (PPSU Radel® R5000)<br>- Silicone/ Polydimethylsiloxane<br>BEGO Semados® DSTr 58356/<br>BEGO SEMADOS® PKTr 58357:<br>- Polyphenylsulfone (PPSU Radel® R5000<br>- Polypropylene Heat Stabilized (PP-HS) | Polyphenylsulfone (Radel® R5000)<br>Silicone | Similar | |
| Material compatibility with sterilization process | Yes | Yes | Identical | |
| Enclosing feature | BEGO SEMADOS® Tr 58350/ BEGO Semados® Tr 58349: Silicone rubber grommets | Silicone grommets | Similar | |
| | | Subject Device | Predicate Device | |
| Feature | | BEGO Semados® Trays (K201412) | Straumann BLX Surgical Cassette<br>(K180791) | Comparison |
| | | BEGO Semados® DSTr 58356/ BEGO SEMADOS® PKTr 58357: None | | |
| Dimension | Device Model | Dimension [mm] | | |
| | BEGO SEMADOS® Tr 58350 | 188.1 x 138.7 x 61.5 | | Different |
| | BEGO Semados® Tr 58349 | 142.7 x 99.6 x 61 | 143 mm x 100 mm x 61 mm | |
| | BEGO Semados® DSTr 58356 | 80 x 85 x 28 | | |
| | BEGO SEMADOS® PKTr 58357 | 140 x 80 x 25 | | |
{12}------------------------------------------------
{13}------------------------------------------------
{14}------------------------------------------------
# Summary of non-clinical testing
Provided below is a summary table of the non-clinical testing that were performed using the subject device. The result demonstrated that the subject device non-clinical test results met the acceptance criteria of the standards.
| | | Non-Clinical Performance Testing Table |
|--|--|----------------------------------------|
|--|--|----------------------------------------|
| Test/ Methodology | Purpose | Acceptance Criteria | Results |
|---------------------------------------------------------------------------------|---------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| AAMI TIR30:2011 | Automated Cleaning<br>Validation – Protein<br>Analysis | Verify cleaning instruc-<br>tions provided are effi-<br>cacious for removing<br>gross amounts of soil to<br>a residual protein level<br>of 6.4 µg protein/cm² | The automated cleaning validation of<br>BEGO Semados® Trays concluded that the<br>manufacturer's cleaning instructions are<br>efficacious for removing gross amounts of<br>soil to a residual protein level of 6.4 µg<br>protein/cm². |
| AAMI TIR30:2011 | Automated Cleaning<br>Validation - Organic<br>Carbon Analysis | Verify cleaning instruc-<br>tions provided are effi-<br>cacious for removing<br>gross amounts of soil to<br>a total organic carbon<br>(TOC) content of 3.1 µg<br>of C/cm² | The automated cleaning validation of<br>BEGO Semados® Trays concluded that the<br>manufacturer's cleaning instructions are<br>efficacious for removing gross amounts of<br>soil to a total organic carbon (TOC) con-<br>tent of 3.1 µg of C/cm2. |
| ISO 10993-5:2009 | Cell Growth Analysis<br>via XTT-Staining | Verify the device does<br>not have a cytotoxic po-<br>tential. An inhibition of<br>cell growth (ICG) of<br>more than 30% is con-<br>sidered as cytotoxic ef-<br>fect. | The cytotoxicity testing concluded that<br>test devices met the requirements of the<br>test and are not considered to have a cy-<br>totoxic potential. |
| ISO 17665-1:2006-<br>08<br>ISO TS 17665-<br>2:2009-01<br>ANSI/AAMI<br>ST77:2013 | Sterilization validation | Verify the device and<br>cycle parameters<br>achieve a Sterility As-<br>surance Level (SAL) of<br>10-6. | The tested devices achieved a SAL of 10-6<br>after processing in pre-vacuum steam<br>sterilization cycle at 132°C for 4 minutes. |
| AAMI TIR12:2010 | Drying Time testing | Verify the device is<br>properly dried using the<br>specified cycle parame-<br>ters. | The BEGO Semados® Trays are considered<br>properly dried following processing in<br>pre-vacuum steam sterilization cycle at<br>132°C for 4 minutes, and drying time of<br>20 minutes. |
## Conclusion
The conclusions drawn from the non-clinical tests demonstrate that the BEGO SEMADOS® Tr 58350, BEGO Semados® Tr 58349, BEGO Semados® DSTr 58356, BEGO SEMADOS® PKTr 58357 Device is as safe, as effective, and performs as well as or better than the legally marketed predicate device, Straumann BLX Surgical Cassette.
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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.