Medical Device Manufacturer · US , Medley , FL

OSTEOMNI, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2026

Total

Cleared

Denied

OSTEOMNI, Inc. has 2 FDA 510(k) cleared medical devices. Based in Medley, US.

Latest FDA clearance: May 2026. Active since 2026. Primary specialty: Orthopedic.

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

OSTEOMNI, Inc. 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 - OSTEOMNI, Inc.

2 devices

1-2 of 2