FDA Device Intelligence
Home › ALPHATEC SPINE, INC. › IdentiTi

IdentiTi

ALPHATEC SPINE, INC. · Model 123-12093520 · UDI-DI 00190376246765

PHMMAX Prescription
1
510(k) clearances
23
Adverse events
0
Recalls
81
Facilities

Description

IDENTiTi PC POROUS Ti TRIAL, 12 x 9 x 35mm, 20°

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.