FDA Device Intelligence
Home › NEWCLIP TECHNICS › Newclip Instruments

Newclip Instruments

NEWCLIP TECHNICS · Model ANC177 · UDI-DI 03700569626877

HYA
0
510(k) clearances
11
Adverse events (1 deaths)
1
Recalls
105
Facilities

Recalls

DateFirmReason
2015-06-17Biomet, Inc.Medium Bone Plate Forceps was assembled with the incorrect grip arm tip. Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone.

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.