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iBOT(R) iBOT PMD

by Mobius Mobility

iBOT(R) iBOT PMD is a wheelchair electric-motor-driven propulsion system (FDA Class II) made by Mobius Mobility, listed in FDA GUDID since 6 Jun 2022 (UDI-DI 00857584008010), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00857584008010 UDI-DI Date6 Jun 2022ListedStatusListed 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  • Withdrawn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

Trade name
iBOT(R)
Generic name
Wheelchair electric-motor-driven propulsion system
Model / reference
iBOT PMD
Primary DI / UDI-DI
00857584008010
FDA product code
IMK, ITI
GMDN term
Wheelchair electric-motor-driven propulsion system
Device class
Class II
Regulation number
890.3890, 890.3860
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible

Similar devices

Other devices filed under FDA product code ITI.

Other devices from Mobius Mobility

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)