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

IdentiTi

ALPHATEC SPINE, INC. · Model 130-10342410 · UDI-DI 00190376197876

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

Description

ALIF Trial, 10 x 34 x 24 mm, 10°

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.