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Skintx 90015FIT

by Gd Care Inc.

Skintx 90015FIT is a Class I device made by Gd Care Inc., listed in FDA GUDID since 29 Sep 2022 (UDI-DI B75490015FIT0), 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 NumberB75490015FIT0 UDI-DI Date29 Sep 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Skintx
Generic name
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial
Model / reference
90015FIT
Primary DI / UDI-DI
B75490015FIT0
FDA product code
LYY
GMDN term
Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial
Device class
Class I
Regulation number
880.6250
GUDID distribution status
In Commercial Distribution

Related devices

Category: Hevea-latex examination/treatment glove, non-powdered, non-antimicrobial

Similar devices

Other devices filed under FDA product code LYY (Latex Patient Examination Glove).

Other devices from Gd Care Inc.

See all devices from Gd Care Inc. →

Properties

  • Single use
  • Contains latex
  • Over-the-counter
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (9, all answered No)