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Ssw Endo 23023

by SS White Burs LLC

Ssw Endo 23023 is a Class I device made by SS White Burs LLC, listed in FDA GUDID since 19 Feb 2025 (UDI-DI D690230232), 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 NumberD690230232 UDI-DI Date19 Feb 2025ListedStatusListed 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  • Withdrawn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
Ssw Endo
Generic name
Natural gutta-percha
Model / Ref / Catalog
23023
Primary DI / UDI-DI
D690230232
FDA product code
EKM
GMDN term
Natural gutta-percha
Device class
Class I
Regulation number
872.3850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Natural gutta-percha

Other devices from SS White Burs LLC

See all devices from SS White Burs LLC →

Properties

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