FDA Device Intelligence
HomeFUSION ORTHOPEDICS, LLC › FibFix

FibFix

FUSION ORTHOPEDICS, LLC · Model FN-TH-9050-S · UDI-DI 00840124517455

JDT Prescription
1
510(k) clearances
8
Adverse events
0
Recalls
10
Facilities

Description

End Cap Threaded 7.4mm x 5mm (Sterile)

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.