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

IdentiTi II

ALPHATEC SPINE, INC. · Model 800-10184500-S · UDI-DI 00190376722016

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

Description

IDENTITI II LIF 10 X 18 X 45 MM, 0°

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.