K211721 · Inter-Med, Inc. · NYL · Dec 2, 2021 · Dental
Device Facts
Record ID
K211721
Device Name
PS System
Applicant
Inter-Med, Inc.
Product Code
NYL · Dental
Decision Date
Dec 2, 2021
Decision
SESE
Submission Type
Traditional
Regulation
21 CFR 872.4200
Device Class
Class 1
Attributes
Therapeutic
Indications for Use
The PS System is intended for the delivery and evacuation of endodontic irrigation solutions during root canal procedures.
Device Story
PS System is a closed-system negative pressure irrigation apparatus for root canal procedures. It uses a light-curable barrier to create an airtight seal between the tooth and a stage; irrigant is delivered and then evacuated via the dental chair vacuum system. This process draws fluid toward the coronal chamber, preventing apical irrigant extrusion. The device is used in dental clinics by licensed dental professionals. It is provided in procedural kits (anterior, premolar, molar) containing a stage, placement tool, cannula set, vacuum line, and irrigation solutions. By maintaining negative pressure, the system facilitates canal cleaning and rinsing while reducing the risk of irrigant extrusion compared to traditional positive-pressure syringe irrigation.
Clinical Evidence
No clinical performance testing was performed. Substantial equivalence is based on non-clinical bench testing, including suction flow rate performance, critical dimension analysis, corrosion testing, simulated canal performance testing, shelf-life verification, and biocompatibility analysis per ISO 7405 and ISO 10993-1.
Technological Characteristics
Negative pressure irrigation apparatus. Components include AISI 304 stainless steel cannulas, light-curable barrier, and vacuum suction adapter. Dimensions: HVE adapter 0.438 in, LVE adapter 0.25 in. Cannula OD 0.0118-0.0125 in. Manual operation via dental chair vacuum. Biocompatibility per ISO 7405/ISO 10993-1. Corrosion testing per ISO 10271. Small-bore connectors per ISO 80369-7. Single-use, non-sterile components.
Indications for Use
Indicated for delivery and evacuation of endodontic irrigation solutions during root canal procedures in patients requiring endodontic treatment. Intended for use by licensed dental professionals.
Regulatory Classification
Identification
A dental handpiece and accessories is an AC-powered, water-powered, air-powered, or belt-driven, hand-held device that may include a foot controller for regulation of speed and direction of rotation or a contra-angle attachment for difficult to reach areas intended to prepare dental cavities for restorations, such as fillings, and for cleaning teeth.
Predicate Devices
EndoVac Apical Negative Pressure Irrigation System (K140685)
{0}------------------------------------------------
Image /page/0/Picture/0 description: The image contains the logo of the U.S. Food and Drug Administration (FDA). On the left is the Department of Health & Human Services logo. To the right of that is the FDA logo in blue, with the words "U.S. FOOD & DRUG" stacked on top of the word "ADMINISTRATION".
December 2, 2021
Inter-Med, INC. Brett Arand Senior Product Development Engineer 2200 South Street Racine, Wisconsin 53404
Re: K211721-S002
Trade/Device Name: PS System Regulation Number: 21 CFR 872.4200 Regulation Name: Dental Handpiece And Accessories Regulatory Class: Class I, reserved Product Code: NYL Dated: May 21, 2021 Received: June 4, 2021
Dear Brett Arand:
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 requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part
{1}------------------------------------------------
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,
For Michael E. Adjodha, M.ChE. Assistant Director DHT1B: Division of Dental and ENT Devices OHT1: Office of Ophthalmic, Anesthesia, Respiratory, ENT and Dental Devices Office of Product Evaluation and Quality Center for Devices and Radiological Health
Enclosure
{2}------------------------------------------------
## Indications for Use
510(k) Number (if known)
## K211721
Device Name
PS System
Indications for Use (Describe)
The PS System is intended for the delivery and evacuation of endodontic irrigation solutions during root canal procedures.
| Type of Use (Select one or both, as applicable) | |
|------------------------------------------------------------------------------------------------|-----------------------------------------------------------------------------------------------|
| <span style="text-decoration: overline;">X</span> Prescription Use (Part 21 CFR 801 Subpart D) | <span style="text-decoration: overline;"> </span> Over-The-Counter Use (21 CFR 801 Subpart C) |
## CONTINUE ON A SEPARATE PAGE IF NEEDED.
This section applies only to requirements of the Paperwork Reduction Act of 1995.
## *DO NOT SEND YOUR COMPLETED FORM TO THE PRA STAFF EMAIL ADDRESS BELOW.*
The burden time for this collection of information is estimated to average 79 hours per response, including the time to review instructions, search existing data sources, gather and maintain the data needed and complete and review the collection of information. Send comments regarding this burden estimate or any other aspect of this information collection, including suggestions for reducing this burden, to:
> Department of Health and Human Services Food and Drug Administration Office of Chief Information Officer Paperwork Reduction Act (PRA) Staff PRAStaff@fda.hhs.gov
"An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number."
{3}------------------------------------------------
Image /page/3/Picture/0 description: The image shows the logo for Intermed INC. The word "intermed" is in a bold, sans-serif font, with the "i" in lowercase and the rest of the letters in uppercase. There is a horizontal line underneath the word "intermed". To the right of the word "intermed" is a globe graphic. To the right of the globe graphic is the word "INC.", which is in a smaller, sans-serif font.
Image /page/3/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features the word "VISTA" in large, bold letters, with the letters slightly overlapping. Above the word "VISTA" is a stylized mountain range. Below the word "VISTA" are the words "Dental Products".
# 510(k) Summary-K211721 PS System
#### 1. Applicant
Inter-Med / Vista Dental Products 2200 South Street Racine, WI, USA 53404
Contact Person: Brett Arand Telephone Number: (262) 633-0755 Fax Number: (262) 636-9760 Email: barand(@vista-dental.com
Date Prepared: November 3rd, 2021 Prepared By: Brett Arand
#### 2. Device Name
| Proprietary Name: | PS System |
|----------------------|--------------------------------------------------------|
| Classification Name: | Handheld controller, air-powered, root canal irrigatio |
| CRF Number: | 872.4200 |
| Product Code: | NYL |
| Device Class: | Class I |
#### 3. Predicate Device
The PS System is substantially equivalent to the legally marketed device Endo Vac Apical Negative Pressure Irrigation System (K140685), submitted by Sybron Endo and cleared on July 2nd, 2014, product code NYL.
### 4. Device Description
The PS System presents a clinically effective way to irrigate the entire canal space during root canal treatments. The PS System is a closed system negative pressure irrigation apparatus that draws fluid through the individually placed cannula toward the coronal chamber by way of evacuation that is controlled independently through the dental chair vacuum system, eliminating the risk of apical irrigant extrusion during root canal procedures. The PS System creates a closed system by establishing an air tight seal between the tooth and stage via a lightcurable barrier. The PS System is designed to accommodate the full range of tooth and root canal anatomy and is offered in three specific procedural kits based on the type of tooth to be treated: anterior, premolar, and molar.
{4}------------------------------------------------
Image /page/4/Picture/0 description: The image shows the logo for Intermed INC. The word "intermed" is written in a sans-serif font, with a line underneath it. To the right of the word is a globe, and to the right of the globe is the word "INC."
Image /page/4/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features a stylized mountain range above the word "VISTA" in a sans-serif font. Below "VISTA" is the phrase "Dental Products" in a smaller font. There is a horizontal line below the word "VISTA".
The PS System is packaged in procedural kits composed of the following items:
| PS System Component | Class | Product<br>Code | FDA Status |
|------------------------------------------------------------------------|-------|-----------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| 1. Stage (molar, premolar or anterior) | | | |
| 2. Placement tool (molar, premolar or<br>anterior) | 1 | NYL | Subject of new 510(k) |
| 3. Cannula set with connection tubing<br>(molar, premolar or anterior) | 1 | NYL | Subject of new 510(k) |
| 4. Vacuum Line with suction adapter | | | |
| 5. Light Curable Barrier | 1 | EIE | Exempt per 21 CFR 872.6300 |
| 6. Sodium hypochlorite with wetting agents<br>(i.e. Chlor-Xtra) | U | KJJ | Reference to Chlor-Xtra cleared<br>in K082470 in light of<br>completed Chlor-Xtra Plus 8%<br>NaOCl Regulatory Change<br>Assessment dated 10/27/2021<br>included in Section 11 - Device<br>DescriptionCleared via K082470 |
| 7. SmearOFF | U | KJJ | Cleared via K193409 |
| 8. Syringe | 1 | EIC | Premarket notification exempt<br>per 21 CFR 872.4565 |
| 9. Application Tips | 1 | EIC | Premarket notification exempt<br>per 21 CFR 872.4565 |
This is the only 510(k) for the PS System medical device, no prior 510(k)s have been submitted.
### ട. Intended Use / Indication for Use
The PS System is intended for the delivery and evacuation of endodontic irrigation solutions during root canal procedures.
#### 6. Technological Characteristics and Substantial Equivalence
The technological characteristics of the PS System are very similar to the predicate EndoVac System (K140685). The PS System and the predicate EndoVac System (K140685) perform the same function, which is a method to deliver irrigant, rinse and evacuate during root canal procedures. A comprehensive comparison of technological characteristics and substantial equivalence between the systems is provided below.
{5}------------------------------------------------
Image /page/5/Picture/0 description: The image shows the logo for Intermed INC. The word "intermed" is in a dark gray sans-serif font, with a line underneath it. To the right of the word is a globe, with the letters "INC." in a smaller font to the right of the globe.
Image /page/5/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features the word "VISTA" in a stylized font, with a mountain range graphic above it. Below the word "VISTA" is the text "Dental Products".
| Table 5-2: Predicate and Proposed Device Comparison Table | | |
|-----------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------|
| | Predicate Device | Proposed Device |
| | EndoVac System | PS System |
| 510(k) | K140685 | K211721 |
| Trade name | EndoVac Apical Negative<br>Pressure Irrigation System | PS System (Molar,<br>Premolar, Anterior) |
| Class | Class 1 | Class 1 |
| FDA Classification<br>Name and CFR<br>Number | Handheld controller, Air-<br>Powered, Root Canal<br>Irrigation<br>872.4200 | Handheld controller, Air-<br>Powered, Root Canal<br>Irrigation<br>872.4200 |
| Product code | NYL | NYL |
| Indication for use /<br>intended use | The EndoVac system is<br>intended for the delivery<br>and evacuation of<br>endodontic irrigation<br>solutions during root canal<br>procedures. | The PS System is intended<br>for the delivery and<br>evacuation of endodontic<br>irrigation solutions during<br>root canal procedures. |
| Target Users | Licensed Dental<br>Professionals | Licensed Dental<br>Professionals |
| Anatomical site | Oral cavity / Isolated tooth | Oral cavity / Isolated tooth |
Inter-Med, Inc. | 2200 South Street, Racine, WI 53404
{6}------------------------------------------------
Image /page/6/Picture/0 description: The image shows the logo for Intermed INC. The word "intermed" is written in a bold, sans-serif font, with a line underneath it. To the right of the word "intermed" is a globe graphic, and to the right of the globe is the word "INC" in a smaller, sans-serif font.
Image /page/6/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features the word "VISTA" in a stylized font, with a mountain range graphic above it. Below the word "VISTA" is the text "Dental Products" in a smaller font. There is a horizontal line below the word "VISTA".
| | Predicate Device | Proposed Device |
|-------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|----------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | EndoVac System | PS System |
| Device Components | Syringes, Multi-Port<br>Adapter, Master Delivery<br>Tip, Fingerpiece, Handheld<br>controller, MicroCannula<br>and MacroCannula,<br>Connection tubing | Stage (molar, premolar or anterior), Cannula with<br>Connection Tubing (molar,<br>premolar or anterior),<br>Vacuum Line with suction<br>adapter, VacuSeal Light<br>Curable Barrier, Sodium<br>hypochlorite with wetting<br>agents (i.e. Chlor-Xtra),<br>SmearOFF, Syringes and<br>Application Tips |
| Vacuum Connection | Multi-Port Adapter | Suction Adapter (fits both<br>HVE and LVE) |
| Suction Adapter<br>Dimensions | The Multi-Port Adapter<br>critical to functionality<br>dimension in this<br>component is the Outer<br>Diameter (OD) due to<br>compatibility with dental<br>chair high evacuation line<br>(OD = 0.434 in) | The Suction Adapter<br>critical to functionality<br>dimension in this<br>component is the Outer<br>Diameter (OD) due to<br>compatibility with dental<br>chair evacuation line<br>HVE adapter: 0.438 in ±<br>0.01 in<br>LVE adapter: 0.25 in ± 0.01<br>in |
{7}------------------------------------------------
Image /page/7/Picture/0 description: The image shows the logo for Intermed INC. The word "intermed" is in a bold, sans-serif font, with a horizontal line underneath. To the right of the word is a globe graphic, and the letters "INC" are to the right of the globe.
Image /page/7/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features the word "VISTA" in a stylized font, with a mountain range graphic above it. Below the word "VISTA" is the text "Dental Products" in a smaller font. There is a horizontal line below the word "VISTA".
| | Predicate Device | Proposed Device |
|---------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | EndoVac System | PS System |
| Cannula Dimensions | MicroCannula critical to<br>functionality dimension in<br>this component is the OD<br>due to the clinical<br>application into the root<br>canal cleaning procedure<br>(OD = 0.0125 to 0.0118 in) | The Cannula critical to<br>functionality dimension in<br>this component is the OD<br>due to the clinical<br>application into the root<br>canal cleaning procedure<br>(OD = 0.0125 to 0.0118 in) |
| Cannula Working<br>Length | MicroCannula working<br>length is from 14 to 30 mm<br>± 0.5 mm | Cannula working length is<br>greater than 30mm |
| Cannula Material | MicroCannula: AISI 304<br>Stainless Steel | AISI 304 Stainless Steel |
| Mode of Operation | Manually operated | Manually operated |
| Fluid Delivery System | Manual operation of<br>syringe plunger (i.e.<br>positive pressure from user) | Manual operation of the<br>dental chair vacuum system<br>(i.e. negative pressure<br>suction from dental chair<br>vacuum) |
| Liquids & Storage | • 20 ml syringe NaOCl<br>• 3 ml syringe EDTA | • 100mL (molar), 60mL (pre-<br>molar), 40mL (anterior)<br>solution pouch Chlor-Xtra<br>Plus<br>• 3ml syringe SmearOFF |
{8}------------------------------------------------
Image /page/8/Picture/0 description: The image shows the logo for Intermed INC. The word "intermed" is written in a bold, sans-serif font, with a line underneath it. To the right of the word "intermed" is a globe, and to the right of the globe is the word "INC" in a smaller font.
Image /page/8/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features the word "VISTA" in a stylized font, with a mountain range graphic above it. Below the word "VISTA" is the text "Dental Products" in a smaller font. There is a horizontal line to the left of the word "VISTA".
| | Predicate Device | Proposed Device |
|-------------------------------------------------------------------|--------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | EndoVac System | PS System |
| Unclogging<br>Mechanism | Requires MacroCannula<br>and MicroCannula to be<br>disconnected from the<br>vacuum line. The<br>MacroCannula and<br>MicroCannula are<br>independently connected to<br>another syringe and<br>positive pressure is applied<br>to dislodge and unclog any<br>debris. | The cannula are connected<br>to a syringe and positive<br>pressure is applied to<br>dislodge and unclog any<br>debris by rotating stop-cock<br>on tubing manifold,<br>however since fluid is<br>drawn out of the cannula<br>and not through the cannula<br>clogging is drastically<br>reduced. |
| Cross contamination<br>(cleaning, disinfection,<br>sterilization) | Meet Requirements<br>Patient contacting portion<br>is autoclavable | All components are non-<br>sterile and single use |
| Shelf-Life | NA, no solutions included | Shelf life is 24 months |
| Biocompatibility<br>Testing / Analysis<br>Performed | Meets Requirements | All components that make<br>patient contact have been<br>evaluated according to ISO<br>7405 / ISO 10993-1 and<br>meet requirements |
| Recommended<br>Irrigation Time | Per manufacturer's<br>instruction for use there are<br>3 phases of EndoVac<br>irrigation / evacuation: | There are 2 phases of PS<br>System irrigation /<br>evacuation: |
{9}------------------------------------------------
Image /page/9/Picture/0 description: The image shows the logo for Intermed INC. The logo features the word "intermed" in a bold, sans-serif font, with a line underneath. To the right of the word is a globe graphic, and to the right of the globe is the word "INC" in a smaller, sans-serif font.
Image /page/9/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features a stylized mountain range above the word "VISTA" in a sans-serif font. To the right of the word "VISTA" is the trademark symbol. Below the word "VISTA" are the words "Dental Products".
| | Predicate Device | Proposed Device |
|--------------------|-------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------|
| | EndoVac System | PS System |
| | (1) Gross evacuation during<br>orifice expansion and<br>between instrument<br>changes, as needed<br>(2) Macro evacuation after<br>complete instrumentation,<br>30 second for each canal<br>(3) Micro evacuation at full<br>WL, 3 cycles each 70-90<br>seconds for each canal.<br>Total irrigation time per<br>canal is 250 seconds,<br>therefore 4 roots: 1000<br>seconds (16:40 minutes) | (1) Gross evacuation during<br>orifice expansion and<br>between instrument<br>changes, as needed<br>(2) Multi-cannular<br>irrigation once stage has<br>been sealed,<br>Total irrigation time for any<br>number of canals is<br>approximately 15-20<br>minutes |
| Prescription / OTC | Prescription | Prescription |
## Applicable Standards
ISO 7405 - Dentistry - Evaluation of biocompatibility of medical devices used in dentistry
ISO 14971 – Application of Risk Management to Medical Devices ISO 80369-7 - Small-bore connectors for liquids and gases in healthcare applications - Part 7: Connectors for intravascular or hypodermic applications ISO 10271 - Dentistry - Corrosion test methods for metallic materials
### Non-Clinical Performance Testing and Compliance 7.
The technological characteristics of the PS System are very similar to the predicate EndoVac (K140685) negative pressure irrigation system. The PS System and the predicate EndoVac System (K140685) perform the same function, which is a method to
{10}------------------------------------------------
Image /page/10/Picture/0 description: The image shows the logo for Intermed INC. The logo features the word "intermed" in a bold, sans-serif font, followed by "INC." in a smaller font. To the right of the text is a globe graphic, with lines of latitude and longitude. A horizontal line underlines the text.
Image /page/10/Picture/1 description: The image shows the logo for Vista Dental Products. The logo features the word "VISTA" in large, bold letters, with a mountain range graphic above it. Below the word "VISTA" is the phrase "Dental Products" in smaller letters. There is also a horizontal line below the phrase "Dental Products".
deliver irrigant, rinse and evacuate during root canal procedures. The following performance tests were conducted as part of design verification:
- Suction Flow Rate Performance
- Critical Dimensions for Clinical Performance Analysis ●
- Corrosion Testing ●
- Simulated Canal Performance Testing ●
- Shelf Life Verification ●
- . Biocompatibility Analysis
- Transit Testing ●
- Additive Manufacturing Summary Document
### Clinical Performance Data 8.
Clinical performance testing has not been performed for the PS System.
### 9. Conclusion as to Substantial Equivalence
The proposed PS System and the predicate EndoVac System (K140685) have the same Indications for Use (besides trade name), which is, for the delivery and evacuation of endodontic irrigation solutions during root canal procedures. The PS System and the predicate EndoVac System (K140685) perform the same function, which is a method to deliver irrigant, rinse and evacuate during root canal procedures. The PS System and the EndoVac System are both negative pressure irrigation apparatuses that reduce the risk of apical extrusion compared to convention positive pressure syringe irrigation.
The technological characteristics of the PS System are very similar to the predicate EndoVac System (K140685). The proposed PS System is substantially equivalent to the predicate EndoVac System (K140685) based on design, performance, technological characteristics use of biocompatible materials, indications for use and the intended use. Any noted differences in technological characteristics between the proposed and predicate devices do not raise any new questions of safety and effectiveness. Based on extensive comparative analysis and testing the PS System is substantially equivalent to the predicate EndoVac System (K140685).
Predicate graph will load when search results are available.
Embedding visualization will load when search results are available.
PDF viewer will load when search results are available.
Loading panels...
Select an item from Submissions
Click any panel, subpart, regulation, product code, or device to see details here.
Section Matches
Results will appear here.
Product Code Matches
Results will appear here.
Special Control Matches
Results will appear here.
Loading collections...
Loading
My Alerts
You will receive email notifications based on the filters and frequency you set for each alert.
Sort by:
Create Alert
Search Filters
Agent Token
Create a read-only bearer token for Claude, ChatGPT, or other agents that can call HTTP APIs.
Copy this now. It will not be shown again.
Connected apps
Apps you authorized through browser sign-in. Disconnecting revokes their access immediately.
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.