Medical Device Manufacturer · US , Ashland , MA

Kepler Medtec - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Kepler Medtec has 2 FDA 510(k) cleared medical devices. Based in Ashland, US.

Historical record: 2 cleared submissions from 2010 to 2011. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Kepler Medtec Filter by specialty or product code using the sidebar.

Kepler Medtec is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Kepler Medtec

2 devices

1-2 of 2