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Vive LVA1069BLK

by Vive Health LLC

Vive LVA1069BLK is an assistive lifting/tilting positioning system (FDA Class I; FDA product code IKX, Aid, Transfer) made by Vive Health LLC, listed in FDA GUDID since 16 Oct 2018 (UDI-DI 00818323021080), 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 Number00818323021080 UDI-DI Date16 Oct 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  • Withdrawn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
Vive
Generic name
Assistive lifting/tilting positioning system
Model / reference
LVA1069BLK
Primary DI / UDI-DI
00818323021080
FDA product code
IKX
GMDN term
Assistive lifting/tilting positioning system
Device class
Class I
Regulation number
890.5050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IKX (Aid, Transfer).

Other devices from Vive Health LLC

See all devices from Vive Health LLC →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)