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Thera Plus 64410301

by Fourstar Group Inc.

Thera Plus 64410301 is a Class I device made by Fourstar Group Inc., listed in FDA GUDID since 5 Dec 2024 (UDI-DI 00049696122160), 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 Number00049696122160 UDI-DI Date5 Dec 2024ListedStatusListed 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  • Withdrawn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
Thera Plus
Generic name
First aid kit, non-medicated, reusable
Model / reference
64410301
Primary DI / UDI-DI
00049696122160
FDA product code
OHO
GMDN term
First aid kit, non-medicated, reusable
Device class
Class I
Regulation number
878.4014
GUDID distribution status
In Commercial Distribution

Related devices

Category: First aid kit, non-medicated, reusable

Other devices from Fourstar Group Inc.

See all devices from Fourstar Group Inc. →

Properties

  • Single use
  • Over-the-counter
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)