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BioSonic UC39

by Coltene/Whaledent Inc.

BioSonic UC39 is a Class I device made by Coltene/Whaledent Inc., listed in FDA GUDID since 11 Feb 2019 (UDI-DI D661UC390), 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 NumberD661UC390 UDI-DI Date11 Feb 2019ListedStatusListed 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  • Withdrawn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
BioSonic
Generic name
Ultrasonic-cleaning water bath
Model / reference
UC39
Primary DI / UDI-DI
D661UC390
FDA product code
FLG
GMDN term
Ultrasonic-cleaning water bath
Device class
Class I
Regulation number
880.6150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ultrasonic-cleaning water bath

Similar devices

Other devices filed under FDA product code FLG (Cleaner, Ultrasonic, Medical Instrument).

Other devices from Coltene/Whaledent Inc.

See all devices from Coltene/Whaledent Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)