Home › Corentec Co., Ltd › BENCOX Total Hip System Instrumentation

BENCOX Total Hip System Instrumentation

Corentec Co., Ltd · Model HA.013.0001 · UDI-DI 08800017200446

HXO Prescription

510(k) clearances

Adverse events

Recalls

Facilities

Description

Mirabo Cup Impactor

Recalls

Date	Firm	Reason
2010-08-02	Biomet, Inc.	The firm has received four complaints that the closed knot pusher is missing a radius which contributes to sutures being cut during surgery.

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 key Read 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.