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Edta Solution, 17% EDTA120

by Pulpdent Corporation

Edta Solution, 17% EDTA120 is a Class I device made by Pulpdent Corporation, listed in FDA GUDID since 21 Jul 2016 (UDI-DI D701EDTA1202), 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 NumberD701EDTA1202 UDI-DI Date21 Jul 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  • Withdrawn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
Edta Solution, 17%
Generic name
Endodontic reaming aid material
Model / reference
EDTA120
Description
LIQUID SOLUTION 120 mL bottle
Primary DI / UDI-DI
D701EDTA1202
FDA product code
EKL
GMDN term
Endodontic reaming aid material
Device class
Class I
Regulation number
872.3840
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 120 Milliliter

Similar devices

Other devices filed under FDA product code EKL (Point, Silver, Endodontic).

Other devices from Pulpdent Corporation

See all devices from Pulpdent Corporation →

Properties

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