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Hoveround LX-5

by Hoveround Corp.

Hoveround LX-5 is a wheelchair (FDA Class II; FDA product code ITI, Wheelchair, Powered) made by Hoveround Corp., listed in FDA GUDID since 9 Aug 2018 (UDI-DI 00859781000002), 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 Number00859781000002 UDI-DI Date9 Aug 2018ListedStatusListed 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  • Withdrawn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
Hoveround
Generic name
Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible
Model / reference
LX-5
Primary DI / UDI-DI
00859781000002
FDA product code
ITI
GMDN term
Wheelchair, electric-motor-driven, occupant-controlled, powered-steering, non-collapsible
Device class
Class II
Regulation number
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 (Wheelchair, Powered).

Other devices from Hoveround Corp.

See all devices from Hoveround Corp. →

Properties

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