Skip to content

Inspire INSSVGPF-L

by K2 Health Products LLC

Inspire INSSVGPF-L is a Class I device made by K2 Health Products LLC, listed in FDA GUDID since 10 Aug 2022 (UDI-DI 00816554010262), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816554010262 UDI-DI Date10 Aug 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  • Withdrawn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
Inspire
Generic name
Vinyl examination/treatment glove, non-powdered
Model / reference
INSSVGPF-L
Primary DI / UDI-DI
00816554010262
FDA product code
LYZ
GMDN term
Vinyl examination/treatment glove, non-powdered
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vinyl examination/treatment glove, non-powdered

Other devices from K2 Health Products LLC

See all devices from K2 Health Products LLC →

Properties

  • Single use
  • Over-the-counter
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)