FDA Device Intelligence
HomeOSSIO LTD › OSSIOfiber® Compression Staple

OSSIOfiber® Compression Staple

OSSIO LTD · Model OF1062020S · UDI-DI 07290017630892

MNU Prescription
2
510(k) clearances
30
Adverse events
0
Recalls
14
Facilities

Description

OSSIOfiber® Compression Staple, 20x20 mm. Package contains: 1 Implant.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.