Skip to content

Dental City 39-PE2

by Icp, Inc.

Dental City 39-PE2 is a Class I device made by Icp, Inc., listed in FDA GUDID since 19 Jul 2021 (UDI-DI D77139PE2), 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 NumberD77139PE2 UDI-DI Date19 Jul 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  • Withdrawn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
Dental City
Generic name
Manual endodontic file/rasp, single-use
Model / reference
39-PE2
Primary DI / UDI-DI
D77139PE2
FDA product code
EKP
GMDN term
Manual endodontic file/rasp, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual endodontic file/rasp, single-use

Other devices from Icp, Inc.

See all devices from Icp, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)