FDA Device Intelligence
Home › Tekno-Medical Optik-Chirurgie GmbH › TEKNO®

TEKNO®

Tekno-Medical Optik-Chirurgie GmbH · Model 50459-14 · UDI-DI 04044684066385

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

Description

HARTMANN EAR FORCEPS 14CM

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.