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Cavitron® 82002

by Dentsply Professional

Cavitron® 82002 is a Class II device made by Dentsply Professional, listed in FDA GUDID since 23 Sep 2016 (UDI-DI D003820021), 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 NumberD003820021 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
Cavitron®
Generic name
Ultrasonic dental scaling/debridement system handpiece tip, periodontal
Model / reference
82002
Primary DI / UDI-DI
D003820021
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

Related devices

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

Other devices from Dentsply Professional

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Properties

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