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Vortex Blue Conform Fit VTBGP0425

by Tulsa Dental Products LLC

Vortex Blue Conform Fit VTBGP0425 is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 30 Jun 2021 (UDI-DI D716VTBGP04251), 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 NumberD716VTBGP04251 UDI-DI Date30 Jun 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  • Withdrawn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
Vortex Blue Conform Fit
Generic name
Synthetic gutta-percha
Model / Ref / Catalog
VTBGP0425
Primary DI / UDI-DI
D716VTBGP04251
FDA product code
EKM
GMDN term
Synthetic gutta-percha
Device class
Class I
Regulation number
872.3850
GUDID distribution status
In Commercial Distribution

Related devices

Category: Synthetic gutta-percha

Other devices from Tulsa Dental Products LLC

See all devices from Tulsa Dental Products LLC →

Properties

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