FDA Device Intelligence
Home › Howmedica Osteonics Corp. › Omnifit

Omnifit

Howmedica Osteonics Corp. · Model 1058-0007 · UDI-DI 07613327013603

LTO Prescription
1
510(k) clearances
58
Adverse events (2 deaths)
0
Recalls
0
Facilities

Description

Proximal Cement Spacer

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.