Medical Device Manufacturer · US , Sarasota , FL

Groupe Lepine - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1999

Total

Cleared

Denied

Groupe Lepine has 2 FDA 510(k) cleared medical devices. Based in Sarasota, US.

Historical record: 2 cleared submissions from 1999 to 2000. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Groupe Lepine

2 devices

1-2 of 2

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: Apr 28, 2026