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Lexicon SSK00821

by Tulsa Dental Products LLC

Lexicon SSK00821 is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 26 Aug 2022 (UDI-DI D716SSK008211), 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 NumberD716SSK008211 UDI-DI Date26 Aug 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  • Withdrawn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
Lexicon
Generic name
Manual endodontic file/rasp, reusable
Model / Ref / Catalog
SSK00821
Primary DI / UDI-DI
D716SSK008211
FDA product code
EKS
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

Similar devices in this category

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

Other devices from Tulsa Dental Products LLC

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Properties

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