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UGen Movement Intelligence Platform 003

by Xperience Robotics Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860015373113 UDI-DI Date28 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
UGen Movement Intelligence Platform
Generic Name
Biomechanical function analysis/rehabilitation software
Model / Reference
003
Primary DI / UDI-DI
00860015373113
FDA Product Code
QKC
GMDN Term
Biomechanical function analysis/rehabilitation software
Device Class
Class II
Regulation Number
890.5360
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Properties

  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date

Other properties (8)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Manufacturing Date: No