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Endo Activator EAPART10

by Tulsa Dental Products LLC

Endo Activator EAPART10 is a Class I device made by Tulsa Dental Products LLC, listed in FDA GUDID since 24 Oct 2022 (UDI-DI D716EAPART101), 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 NumberD716EAPART101 UDI-DI Date24 Oct 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  • Withdrawn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
Endo Activator
Generic name
Ultrasonic dental scaling/debridement system handpiece tip, endodontic
Model / Ref / Catalog
EAPART10
Primary DI / UDI-DI
D716EAPART101
FDA product code
JET
GMDN term
Ultrasonic dental scaling/debridement system handpiece tip, endodontic
Device class
Class I
Regulation number
872.6650
GUDID distribution status
In Commercial Distribution
Sterilisation method
Liquid Chemical

Related devices

Category: Ultrasonic dental scaling/debridement system handpiece tip, endodontic

Other devices from Tulsa Dental Products LLC

See all devices from Tulsa Dental Products LLC →

Properties

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