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WHILL Model M

by Whill, Inc.

WHILL Model M, an electric-motor-driven wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Whill, Inc., was listed in FDA GUDID on 3 Oct 2016 (UDI-DI 00866917000201); the registry lists it as not in commercial distribution (GUDID) as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00866917000201 UDI-DI Date3 Oct 2016ListedStatusListed 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  • Withdrawn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
Whill
Generic name
Electric-motor-driven wheelchair, occupant-controlled
Model / reference
Model M
Primary DI / UDI-DI
00866917000201
FDA product code
ITI
GMDN term
Electric-motor-driven wheelchair, occupant-controlled
Device class
Class II
Regulation number
890.3860
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code ITI (Wheelchair, Powered).

Other devices from Whill, Inc.

See all devices from Whill, Inc. →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)