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Etch Rite ET-3

by Pulpdent Corporation

Etch Rite ET-3 is a Class II device made by Pulpdent Corporation, listed in FDA GUDID since 17 May 2021 (UDI-DI D701ET32), 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 NumberD701ET32 UDI-DI Date17 May 2021ListedStatusListed 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  • Withdrawn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
Etch Rite
Generic name
Dental tooth-etching solution
Model / Ref / Catalog
ET-3
Primary DI / UDI-DI
D701ET32
FDA product code
EBF
GMDN term
Dental tooth-etching solution
Device class
Class II
Regulation number
872.3690
GUDID distribution status
In Commercial Distribution

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Properties

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