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

Ambler Surgical

AMBLER SURGICAL CORP. · Model Iris retractors · UDI-DI 00190660201722

HNI Prescription
2
510(k) clearances
27
Adverse events
0
Recalls
159
Facilities

Description

Iris retractors, flat, bright blue, flexible polypropylene fiber, vertically packaged, sterile, disposable, 1 pack of 5 retractors

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.