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Topex® Prophy Paste AD30000FG

by Dentsply International

Topex® Prophy Paste AD30000FG is a Class I device made by Dentsply International, listed in FDA GUDID since 21 Sep 2016 (UDI-DI D687AD30000FG1), 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 NumberD687AD30000FG1 UDI-DI Date21 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  • Withdrawn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
Topex® Prophy Paste
Generic name
Dentifrice
Model / Ref / Catalog
AD30000FG
Primary DI / UDI-DI
D687AD30000FG1
FDA product code
EJR
GMDN term
Dentifrice
Device class
Class I
Regulation number
872.6030
GUDID distribution status
In Commercial Distribution

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Category: Dentifrice

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Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)