FDA Device Intelligence
Home › Kohler Medizintechnik GmbH › KOHDENT

KOHDENT

Kohler Medizintechnik GmbH · Model 3060 · UDI-DI 04251436904233

EMS Prescription
7
510(k) clearances
23
Adverse events
0
Recalls
92
Facilities

Description

PA-Curettes Goldman-Fox GF5 hollow-ha

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.