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Merete GmbH · Model FH10905 · UDI-DI 04048266076687

HXP Prescription
5
510(k) clearances
156
Adverse events
1
Recalls
158
Facilities

Description

Bending Wrench for Merete Foot system non-sterile

Recalls

DateFirmReason
2013-06-22Synthes USA HQ, Inc.A complaint was received of the tips of the Matrix 5.5.mm Left and Right Coronal Bender breaking while bending a spinal rod component of the Matrix System.

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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.