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TiWedge™

Ascension Orthopedics, Inc. · Model TRL-1006-C06 · UDI-DI 10381780237686

HWC HRS Prescription

510(k) clearances

58,942

Adverse events (75 deaths)

388

Recalls

657

Facilities

Description

The Integra Titanium Bone Wedges are a series of wedge-shaped devices intended to be used for angular correction of small bones in the ankle and foot. The Integra Titanium Bone Wedges are constructed from commercially pure titanium formed into a cancellous-like structure. Trial Cotton 20 X 6.5

Recalls

Date	Firm	Reason
2026-04-24	Medartis AG	The cannulation of the CCS screw is not centered.
2026-01-23	I.T.S. GmbH	Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-23	I.T.S. GmbH	Updated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-09	Medartis AG	Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2026-01-09	Medartis AG	Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2025-11-24	Smith & Nephew, Inc.	Removal of affected lot of screws due to labeling error.
2024-04-12	Medartis Inc.	Screw is 16mm long instead of 22mm long.
2024-03-20	Zimmer, Inc.	Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user sinc
2024-03-20	Zimmer, Inc.	Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user sinc
2024-03-20	Zimmer, Inc.	Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user sinc

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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.