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Streamline PLUS UI30SPXTTB

by Hu-Friedy Mfg Co., LLC

Streamline PLUS UI30SPXTTB is a Class II device made by Hu-Friedy Mfg Co., LLC, listed in FDA GUDID since 11 Oct 2019 (UDI-DI 10889950121150), 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 Number10889950121150 UDI-DI Date11 Oct 2019ListedStatusListed 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  • Withdrawn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
Streamline PLUS
Generic name
Ultrasonic dental scaling/debridement system handpiece tip, periodontal
Model / Ref / Catalog
UI30SPXTTB
Primary DI / UDI-DI
10889950121150
FDA product code
ELC
GMDN term
Ultrasonic dental scaling/debridement system handpiece tip, periodontal
Device class
Class II
Regulation number
872.4850
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Safe

Related devices

Category: Ultrasonic dental scaling/debridement system handpiece tip, periodontal

Other devices from Hu-Friedy Mfg Co., LLC

See all devices from Hu-Friedy Mfg Co., LLC →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)