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Inspire INSBLK8MIL-M

by K2 Health Products LLC

Inspire INSBLK8MIL-M is a Class I device made by K2 Health Products LLC, listed in FDA GUDID since 13 Aug 2026 (UDI-DI 00816554016103), 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 Number00816554016103 UDI-DI Date13 Aug 2026ListedStatusListed 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  • Withdrawn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
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Model / reference
INSBLK8MIL-M
Primary DI / UDI-DI
00816554016103
FDA product code
LZA
GMDN term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

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)