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Astek 116239

by Young Innovations, Inc.

Astek 116239 is a Class I device made by Young Innovations, Inc., listed in FDA GUDID since 18 Oct 2022 (UDI-DI 00843471151037), 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 Number00843471151037 UDI-DI Date18 Oct 2022ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Astek
Generic name
Dental delivery system irrigation handpiece
Model / Ref / Catalog
116239
Primary DI / UDI-DI
00843471151037
FDA product code
ECB
GMDN term
Dental delivery system irrigation handpiece
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code ECB (UNIT, SYRINGE, AIR AND/OR WATER).

Other devices from Young Innovations, Inc.

See all devices from Young Innovations, Inc. →

Properties

  • Sterilise before use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)