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Britedent BSI-2830

by Bright Supply Inc

Britedent BSI-2830 is a Class I device made by Bright Supply Inc, listed in FDA GUDID since 26 Nov 2020 (UDI-DI D974BSI28301), 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 NumberD974BSI28301 UDI-DI Date26 Nov 2020ListedStatusListed 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  • Withdrawn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
Britedent
Generic name
Medicine cup, single-use
Model / reference
BSI-2830
Primary DI / UDI-DI
D974BSI28301
FDA product code
KYX
GMDN term
Medicine cup, single-use
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Similar devices

Other devices filed under FDA product code KYX (Dispenser, Liquid Medication).

Other devices from Bright Supply Inc

See all devices from Bright Supply Inc →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)