FDA Device Intelligence
HomeKohler Medizintechnik GmbH › KOHDENT

KOHDENT

Kohler Medizintechnik GmbH · Model 1136 · UDI-DI 04251436901034

EMG Prescription
10
510(k) clearances
11
Adverse events
1
Recalls
215
Facilities

Description

Extracting Forceps English Mead No. 3

Recalls

DateFirmReason
2008-05-21Biomet Microfixation, Inc.The Biomet Microfixation Obwegeser Ramus Clamp, Wide Right 01-7996 were incorrectly etched as the left part number 01-7997.

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.