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Vive LVA2097SLV

by Vive Health LLC

Vive LVA2097SLV is a bedrail (FDA Class I; FDA product code ILS, Adaptor, Hygiene) made by Vive Health LLC, listed in FDA GUDID since 26 Oct 2021 (UDI-DI 00810041987822), 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 Number00810041987822 UDI-DI Date26 Oct 2021ListedStatusListed 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  • Withdrawn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
Bedrail
Model / reference
LVA2097SLV
Primary DI / UDI-DI
00810041987822
FDA product code
ILS
GMDN term
Bedrail
Device class
Class I
Regulation number
890.5050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ILS (Adaptor, Hygiene).

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)