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Orthex

ORTHOPEDIATRICS CORP. · Model ORTHEXRPS · UDI-DI 00841132179772

OSN Prescription
1
510(k) clearances
22
Adverse events
2
Recalls
38
Facilities

Description

Orthex P&C Software v1.2

Recalls

DateFirmReason
2022-09-12OrthoPediatrics CorpBolt breakage on the head or threaded portion, which may cause loss of strut continuity with frame. This may cause loss of deformity correction and/or disruption of bone regenerati
2017-12-13Smith & Nephew, Inc.In rare circumstances, when surgeons use the software to plan the strut adjustment, an inverted image of the frame is generated by the software. The frame will appear inverted

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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.