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Ultra-Blaster

by Ultradent Products, Inc.

510(k) K980726

Ultra-Blaster is a medical device (FDA Class II; FDA product code KOJ, Airbrush) made by Ultradent Products, Inc., cleared under FDA 510(k) K980726 on 12 May 1998, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK980726 Date12 May 1998ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
KOJ
Device class
Class II
Regulation
21 CFR Part 872.6080
Advisory committee
Dental
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code KOJ (Airbrush).

Other devices from Ultradent Products, Inc.

See all devices from Ultradent Products, Inc. →