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

Innomed, Inc.

INNOMED, INC. · Model 5350-50 · UDI-DI 00840277111487

HWM
3
510(k) clearances
767
Adverse events
0
Recalls
254
Facilities

Description

Lambotte Osteotome 1/2"

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.