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DIA-X FILE 21mm D2

by DiaDent Group International 2 variants

DIA-X FILE 21mm D2 (571-102) is a Class I device made by DiaDent Group International, listed in FDA GUDID since 27 May 2020 (UDI-DI 08806383556873), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08806383556873 UDI-DI Date27 May 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Dia-X File
Generic name
Rotary/reciprocating endodontic file/rasp, reusable
Model / Ref / Catalog
21mm D2, 571-102
Primary DI / UDI-DI
08806383556873
FDA product code
DZA
GMDN term
Rotary/reciprocating endodontic file/rasp, reusable
Device class
Class I
Regulation number
872.4130
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Rotary/reciprocating endodontic file/rasp, reusable

Other devices from DiaDent Group International

See all devices from DiaDent Group International →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)