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MindMotionPRO

by MindMaze SA

510(k) K162748

MindMotionPRO is a Class II device made by MindMaze SA, cleared under FDA 510(k) K162748 on 24 Apr 2017, active as of 9 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 9 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 9 Oct 2026.

Regulatory status

as of registry sync 9 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK162748 Date24 Apr 2017ClearedStatusActive

Official records

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  • Withdrawn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
LXJ
Device class
Class II
Regulation
21 CFR Part 890.5360
Advisory committee
Physical Medicine
FDA decision
SESE Substantially Equivalent

Related clearances

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Similar devices

Other devices filed under FDA product code LXJ (Interactive Rehabilitation Exercise Devices).

Other devices from MindMaze SA

  • MindMotion GO

    Class II