FDA Device Intelligence
Home › AMBLER SURGICAL CORP. › Ambler Surgical

Ambler Surgical

AMBLER SURGICAL CORP. · Model John ALK Pre-Descemet membrane spatula · UDI-DI 00190660210366

HND Prescription
6
510(k) clearances
90
Adverse events
0
Recalls
161
Facilities

Description

John ALK Pre-Descemet membrane spatula, double-ended, angled shafts, round handle

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.