FDA Device Intelligence
Home › INNOMED, INC. › Innomed, Inc.

Innomed, Inc.

INNOMED, INC. · Model 4149-FR · UDI-DI 00840277128317

KIL
1
510(k) clearances
11
Adverse events
0
Recalls
36
Facilities

Description

Ortholucent Fixation Ring (cancel)

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.