Skip to content

mo-Vis P031-23

by mo-Vis

mo-Vis P031-23, an assistive rotating/sliding positioning system (FDA Class I; FDA product code KNN, Components, Wheelchair) made by mo-Vis, was listed in FDA GUDID on 23 Nov 2022 (UDI-DI 05407008320966); the registry lists it as not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05407008320966 UDI-DI Date23 Nov 2022ListedStatusListed GUDID: not in commercial distribution

Official records

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  • Withdrawn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
Assistive rotating/sliding positioning system
Model / reference
P031-23
Primary DI / UDI-DI
05407008320966
FDA product code
KNN
GMDN term
Assistive rotating/sliding positioning system
Device class
Class I
Regulation number
890.3920
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code KNN (Components, Wheelchair).

Other devices from mo-Vis

See all devices from mo-Vis →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)