Skip to content

Twister

by Pride Mobility Products Corporation

Twister is an assistive input-control operation training device (FDA Class I; FDA product code KNO, Accessories, Wheelchair) made by Pride Mobility Products Corporation, listed in FDA GUDID since 26 Aug 2019 (UDI-DI 00606509900140), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00606509900140 UDI-DI Date26 Aug 2019ListedStatusListed GUDID: 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  • Withdrawn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

Generic name
Assistive input-control operation training device, selection techniques
Model / Ref / Catalog
TWISTER
Primary DI / UDI-DI
00606509900140
FDA product code
KNO
GMDN term
Assistive input-control operation training device, selection techniques
Device class
Class I
Regulation number
890.3910
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KNO (Accessories, Wheelchair).

Other devices from Pride Mobility Products Corporation

See all devices from Pride Mobility Products Corporation →

Properties

  • Prescription use
  • Over-the-counter
  • Premarket exempt
  • Serial number
Other properties (11, all answered No)