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Integra® TruArch®

Ascension Orthopedics, Inc. · Model TRUARCHIMP · UDI-DI 10381780074342

HWC Prescription
1
510(k) clearances
58,942
Adverse events (75 deaths)
388
Recalls
657
Facilities

Description

The Integra TruArch subtalar implant is a one-piece titanium implant for treating hyperpronation of the foot. It is designed to block forward, downward and medial displacement of the talus, thus allowing normal subtalar joint motion but blocking excessive pronation and the resulting sequela. The implant is offered in 5 sizes ranging from 8mm to 12mm in diameter. The system includes instruments to facilitate the placement of the implants.

Recalls

DateFirmReason
2026-04-24Medartis AGThe cannulation of the CCS screw is not centered.
2026-01-23I.T.S. GmbHUpdated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-23I.T.S. GmbHUpdated MRI safety testing demonstrates higher RF-induced temperature increases under certain MRI conditions than previously reflected in the Instructions for Use (IFU).
2026-01-09Medartis AGMix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2026-01-09Medartis AGMix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
2025-11-24Smith & Nephew, Inc.Removal of affected lot of screws due to labeling error.
2024-04-12Medartis Inc.Screw is 16mm long instead of 22mm long.
2024-03-20Zimmer, 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
2024-03-20Zimmer, 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
2024-03-20Zimmer, 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.