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Endodontic Hand Instruments 82125008

by Tulsa Dental Products LLC

Endodontic Hand Instruments 82125008 is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 19 Nov 2022 (UDI-DI D716821250081), 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 NumberD716821250081 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  • Withdrawn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, reusable
Model / Ref / Catalog
82125008
Primary DI / UDI-DI
D716821250081
FDA product code
EKP
GMDN term
Manual endodontic file/rasp, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Manual endodontic file/rasp, reusable

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Other devices filed under Manual endodontic file/rasp, reusable.

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Properties

  • Supplied sterile
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)