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Endodontic Hand Instruments 5325020

by Tulsa Dental Products LLC 29 variants

Endodontic Hand Instruments 5325020 (5325050) is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 19 Nov 2022 (UDI-DI D716053250501), 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 NumberD716053250501 UDI-DI Date19 Nov 2022ListedStatusListed 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  • Withdrawn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
Endodontic Hand Instruments
Generic name
Manual endodontic file/rasp, single-use
Model / Ref / Catalog
5325020, 5325050
Primary DI / UDI-DI
D716053250501
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 Tulsa Dental Products LLC

See all devices from Tulsa Dental Products LLC →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)