FDA Device Intelligence
HomeHNM STAINLESS, LLC. › HNM MEDICAL

HNM MEDICAL

HNM STAINLESS, LLC. · Model HNM-1-63-8850 · UDI-DI 00842962149232

KAE
10
510(k) clearances
82
Adverse events
1
Recalls
224
Facilities

Description

FRONTAL SINUS GIRAFFE FORCEP, 5 1/4", 3MM CUP, VERTICAL 45°

Recalls

DateFirmReason
2025-01-31Aesculap IncThe 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 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.