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mo-vis P002-79 All-round Joystick LiNX Light

by mo-Vis

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05407008321260 UDI-DI Date1 Sep 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  • Withdrawn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
mo-vis
Generic Name
Wheelchair steering/control unit
Model / Reference
P002-79 All-round Joystick LiNX Light
Primary DI / UDI-DI
05407008321260
FDA Product Code
KNN
GMDN Term
Wheelchair steering/control unit
Device Class
Class I
Regulation Number
890.3920
GUDID distribution status
In Commercial Distribution

Other devices from mo-Vis

See all devices from mo-Vis →

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No