510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K955050Substantially Equivalent

Jetstream Cavity Preparation System

Dove Systems, Inc., Concord CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955050 is the FDA 510(k) clearance record for JETSTREAM CAVITY PREPARATION SYSTEM, a class II device, cleared for Dove Systems, Inc. on under FDA product code KOJ (Airbrush). FDA records list one 510(k) clearance for Dove Systems, Inc. As of , FDA records show no recalls naming K955050.

Clearance record

Decision date
Received
(125 days to decision)
Product code
KOJ Airbrush
Regulation
21 CFR 872.6080
Device class
Class II
Review panel
Dental
Applicant
Dove Systems, Inc. 1000 Burnett Ave., Suite 450, Concord CA
510(k) summary
Summary
Third party review
No

Clearances, product code KOJ

Trailing 12 months

FDA records hold no clearances under product code KOJ in the trailing twelve months.

FDA records show no clearances under product code KOJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KOJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260