Our role-based focus
Regulatory Specialist
Simplify Compliance and Speed Up FDA Approvals
Navigating complex regulatory pathways can slow down approvals and increase costs. MedTech Tracker streamlines this process with analyzed regulatory data.
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Your Challenges
- Needs to review large amounts of data for regulatory submissions
- Responsible for both pre-submission and post-approval compliance
- Finding the right product codes is difficult
- Manual research wastes time
- Regulatory updates are hard to track
How MedTech Tracker Helps
- Summarized key regulatory data, including adverse event reports.
- Provides access to previous filings for reference
- Supplies full texts of 510(k) and PMA approvals
- Business Navigation Tool that helps you find the correct product codes instantly.
- Adverse Event Monitoring used to Track safety trends
How to Get Started
Download free samples

510K PDF
This is a 510(k) premarket notification for the device Muscle and Nerve Stimulator TENS & EMS (TP2208), Muscle and Nerve with product code NUH, NGX

510K PDF
This PDF contains the 510(k) premarket notification of intent to market the device Transcutaneous Electronic Nerve Stimulator for product code NUH, NYN.

EXCEL WITH MAUDE SUMMARY
This file contains information from FDA’s MAUDE dataset for device code GZJ. It contains these sheets: 510ks: List of 510(k)s for this product code; MDR Numbers: Identifiers for adverse events assigned to this product code and the MDR_xxxx: A separate sheet with full details of each MDR.

510K PDF
510(k) premarket notification of intent to market the device Nooro Body & Foot Stimulator with Product Code: NUH, NGX, NYN, GZJ, IPF

EXCEL WITH PUBMED SUMMARY
This file contains information from PubMed and the content is limited to the term ‘’TENS’’
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MedTech Reference Guide
Gain a better understanding of your product code, access essential medicare data and reimbursement codes. Download the MedTech Reference Guide today and request your free Regulatory and Reimbursement Report to stay ahead in the industry.
