FDA Device Intelligence
Home › GLOBUS MEDICAL, INC. › HEDRON

HEDRON

GLOBUS MEDICAL, INC. · Model 1212.3313S · UDI-DI 00193982649999

PHMMAX
3
510(k) clearances
23
Adverse events
0
Recalls
81
Facilities

Description

HEDRON IA Spacer, 29x39, 13mm, 20°, Convex

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.