Skip to content

Jetstream 115 V

by Deldent Ltd.

Jetstream 115 V (506300) is a Class II device made by Deldent Ltd., cleared under FDA 510(k) K014252 on 19 Feb 2002 and listed in FDA GUDID since 7 Jun 2023 (UDI-DI 07290016281842), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K014252

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290016281842 UDI-DI Date7 Jun 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK014252 Date19 Feb 2002DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K014252 decided 19 Feb 2002 Active
  • FDA GUDID UDI-DI 07290016281842 listed 7 Jun 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K014252
  2. Listed FDA GUDID 07290016281842

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Jetstream
Generic name
Chairside dental abrasive air jet system
Model / Ref / Catalog
115 V, 506300
Primary DI / UDI-DI
07290016281842
510(k) Number
FDA product code
KOJ
GMDN term
Chairside dental abrasive air jet system
Device class
Class II
Regulation number
872.6080
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental abrasive air jet system

Other devices from Deldent Ltd.

See all devices from Deldent Ltd. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Serial number
Other properties (11, all answered No)