FDA Device Intelligence
HomeAvalign Technologies, Inc. › Millennium

Millennium

Avalign Technologies, Inc. · Model 1-380156 · UDI-DI 00190776304584

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

Description

Hartmann Alligator Ear Forceps 6 12" serrated, straight

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.