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The BLASTER BC-B5010

by Micron Corp.

The BLASTER BC-B5010 is a Class I device made by Micron Corp., listed in FDA GUDID since 22 Dec 2022 (UDI-DI 04560205914251), 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 Number04560205914251 UDI-DI Date22 Dec 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  • Withdrawn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
The BLASTER
Generic name
Dental abrasive air jet system handpiece
Model / reference
BC-B5010
Primary DI / UDI-DI
04560205914251
FDA product code
EFB
GMDN term
Dental abrasive air jet system handpiece
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental abrasive air jet system handpiece

Similar devices

Other devices filed under FDA product code EFB (Handpiece, Air-Powered, Dental).

Other devices from Micron Corp.

See all devices from Micron Corp. →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)