Home › AMBLER SURGICAL CORP. › Ambler Surgical
Ambler Surgical
AMBLER SURGICAL CORP. · Model Frontal sinus recess giraffe forceps · UDI-DI 00190660052829
KAE
Prescription
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities
Description
Frontal sinus recess giraffe forceps, working length 125mm, curved up 90 degrees, double-action, 2.0mm vertical cup jaws, ring handle
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
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 docsData 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.