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restor3d Kinos Axiom PSR

Restor3d, Inc. · Model 5831-9003 · UDI-DI 00840097508948

OYK
1
510(k) clearances
11
Adverse events
2
Recalls
12
Facilities

Description

Axiom Talar PSR

Recalls

DateFirmReason
2026-07-27restor3d Inc.Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fix
2011-11-17Integra LifeSciences Corp.During 6/30/2010 to 8/17/2011 the firm received five (5) incident complaints of breakage of the threaded part of the compression guide which potentially occurred when: 1) a compre

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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.