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devemed GmbH · Model 3130 · UDI-DI 04061644013678

HXZ Prescription

510(k) clearances

514

Adverse events

Recalls

247

Facilities

Description

Wire cutter TC | 16 cm for soft wires up to 2.0 mm for hard wires up to 1.6 mm

Recalls

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

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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.