FDA Device Intelligence
HomeGimmi GmbH › Gimmi

Gimmi

Gimmi GmbH · Model KI.1535.15 · UDI-DI 04049047706540

HXZ Prescription
1
510(k) clearances
510
Adverse events
1
Recalls
246
Facilities

Description

WIRE CUTTING PLIER TC, FOR HARD WIRES UP TO Ø 1.5 MM LENGTH 150 MM

Recalls

DateFirmReason
2020-11-20Zimmer Biomet, Inc.Device has the potential for fracture during use.

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.