FDA Device Intelligence
Home › Pro Surgical, Inc. › ProAM ALIF System

ProAM ALIF System

Pro Surgical, Inc. · Model LN-014229-0616 · UDI-DI 00810152902301

LXH Prescription
10
510(k) clearances
82,132
Adverse events (55 deaths)
0
Recalls
1,119
Facilities

Description

ALIF Trial - 42mm x 29mm x 16mm, 6°

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.