Medical Device Manufacturer · US , Leesburg , VA

K2m, LLC - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2005

Total

Cleared

Denied

K2m, LLC has 8 FDA 510(k) cleared medical devices. Based in Leesburg, US.

Historical record: 8 cleared submissions from 2005 to 2018. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by K2m, LLC Filter by specialty or product code using the sidebar.

K2m, LLC 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 - K2m, LLC

8 devices

1-8 of 8