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Delfin2 DELF2-07

by Intra-Lock International

Delfin2 DELF2-07 is a Class I device made by Intra-Lock International, listed in FDA GUDID since 3 Jul 2019 (UDI-DI D742DELF2070), 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 NumberD742DELF2070 UDI-DI Date3 Jul 2019ListedStatusListed 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  • Withdrawn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
Delfin2
Generic name
Dental power tool system handpiece, line-powered
Model / Ref / Catalog
DELF2-07
Primary DI / UDI-DI
D742DELF2070
FDA product code
EKX
GMDN term
Dental power tool system handpiece, line-powered
Device class
Class I
Regulation number
872.4200
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code EKX (Handpiece, Direct Drive, Ac-Powered).

Other devices from Intra-Lock International

See all devices from Intra-Lock International →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)