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Cavitron® 8129502

by Dentsply Professional

Cavitron® 8129502 is a Class II device made by Dentsply Professional, listed in FDA GUDID since 23 Sep 2016 (UDI-DI D00381295021), not in commercial distribution (GUDID) as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 NumberD00381295021 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Model / reference
8129502
Primary DI / UDI-DI
D00381295021
FDA product code
ELC
GMDN term
Ultrasonic dental scaling/debridement system
Device class
Class II
Regulation number
872.4850
GUDID distribution status
Not in Commercial Distribution

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Properties

  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Serial number
Other properties (11, all answered No)