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Blasting Powder Mint

by Bioclear Matrix Systems LLC

Blasting Powder Mint is a Class I device made by Bioclear Matrix Systems LLC, listed in FDA GUDID since 17 Aug 2023 (UDI-DI D949715031121), 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 NumberD949715031121 UDI-DI Date17 Aug 2023ListedStatusListed 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  • Withdrawn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
Blasting Powder
Generic name
Dentifrice
Model / reference
Mint
Primary DI / UDI-DI
D949715031121
FDA product code
EJR
GMDN term
Dentifrice
Device class
Class I
Regulation number
872.6030
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dentifrice

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Other devices filed under Dentifrice.

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Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)