Medical Device Manufacturer · US , Cambridge , MA

The Straumann Co. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1992

Recent clearances: STRAUMANN TEMPORARY COPING, STRAUMANN GRANULES, THE STRAUMANN ORTHO IMPLANT SYSTEM

View 14 510(k) Devices ↓

14

Total

14

Cleared

0

Denied

FDA 510(k) Regulatory Record - The Straumann Co. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Dec 15, 1992

BONE MARROW BIOPSY SYSTEM

General & Plastic Surgery · 134d