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Match Point System

Materialise NV · Model 804-06-351 · UDI-DI 05420060366116

QHEKWSPHX Prescription
1
510(k) clearances
8
Adverse events
2
Recalls
35
Facilities

Description

Guide and Bone model for Reverse Shoulder Arthroplasty (AltiVate® Reverse)

Recalls

DateFirmReason
2026-03-12Linkbio Corp.The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
2021-06-25Tornier S.A.S.Potential patient exposure to the graphite substrate.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.