Mederi Therapeutics, Inc. is one of 19051 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mederi Therapeutics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Stretta Catheter, MEDERI THERAPEUTICS RF GENERATOR CONTROL MODULE
2
Total
2
Cleared
0
Denied
Mederi Therapeutics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Shelton, US.
Historical record: 2 cleared submissions from 2011 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mederi Therapeutics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lakeshore Medical Device Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mederi Therapeutics, Inc.
2 devices