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Trx Vertical Positioner

by Motion Concepts

510(k) K023426

Trx Vertical Positioner is a medical device (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Motion Concepts, cleared under FDA 510(k) K023426 on 21 Nov 2002, active as of 22 Oct 2026. One FDA recall is linked to it.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None ongoing

1 closed

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK023426 Date21 Nov 2002ClearedStatusActive

Official records

Recalls

1 recall · FDA

    • Terminated Z-2657-2014 FDA Class II initiated 28 Aug 2014

    Motion Concepts identified that there is a possibility of knee support failure occurring through fatigue of two attachment bolts in the Vertical Position System (TRx Vertical Positioner).

Timeline

2 dated events

  1. Cleared FDA 510(k) K023426
  2. Recall initiated FDA recalls Z-2657-2014

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
ITI
Device class
Class II
Regulation
21 CFR Part 890.3860
Advisory committee
Physical Medicine
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code ITI (Wheelchair, Powered).

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