Our role-based focus

 

 

 

Each functional area in a MedTech company requires specific types of data, used to perform different types of analysis, and then generates function-specific reports (like a Clinical Evaluation Report, for example).
We have conducted extensive research with MedTech companies to better understand the needs of each of those areas. Our system is designed around the needs of each of these roles, to help them get their job done faster.
This is how we help those in the role of;

Technical Lead

Build Smarter, Safer MedTech Devices with Data-Driven Insights

As a Technical Lead, R&D Engineer, or Product Developer, your focus is building innovative and compliant devices. MedTech Tracker helps you integrate safety, compliance, and market intelligence from day one.

MedTech Roles with airport park concept

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Your Challenges

  • Strong technical skills, but sometimes with little prior experience with MedTech regulations: Regulatory pathways can be confusing.

  • Finding the right regulatory data is difficult: Searching for FDA product codes and approvals takes time.

  • Understanding past failures is challenging: Learning from real-world adverse events can improve safety.

  • Need better manufacturing & compliance insights: Technical teams require detailed device testing, electrical safety, and performance data.

How MedTech Tracker Helps

    • A “Guided Tour” of MedTech Regulations: Navigate FDA approval pathways, safety standards, and compliance requirements step by step.

    • MDR (Medical Device Reporting) Database: Access historical failure reports to reduce risk.

    • Regulatory Data on Similar Devices: Find previously approved products and learn from their testing & manufacturing processes.

    • Manufacturing & Compliance Insights:  Get electrical, safety, and performance testing data for better decision-making.

    How to get started

       

      Download Free Samples

       

      510K Summary for Ascend

      510k PDF

      This is a 510k summary for ASCEND,  intended for use as a transcutaneous electrical nerve stimulation device for temporary relief of pain.

      510k for medical device

      510k PDF

      This is a sample of the 510(k) premarket notification of intent to market the device named Attune division knee system by DePuy Ireland UC

      This file 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 MDR_text: A separate sheet with full details of each MDR.

      510k PDF

      This file 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 MDR_text: A separate sheet with full details of each MDR.

      Over 200,000+ PDFs available. Still Can’t Find What You’re Looking For?

      MedTech Reference Guide

      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.

      "As a technical person, having access to data like indications for use, device descriptions, electrical information, and instructions for use in the PMA document is invaluable. It will directly impact my production and manufacturing processes."

      Oleg

      Technical lead

      Orthosends

      "It also helped me to think for myself and systematize in my head what a technical person really wants."

      Oleg

      Technical lead

      Orthosends