Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: KOJ FDA class 2

Airbrush

Dental

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A Dental Airbrush is a device used in dentistry to deliver a fine, precise stream of air, water, or abrasive particles to the tooth surface for purposes including stain removal, surface preparation, minimally invasive caries removal, and application of dental materials. It is classified as FDA Class 2, indicating moderate risk requiring 510(k) premarket clearance. The product code is KOJ and the applicable regulation is 21 CFR 872.6080 in the Dental specialty. This device is eligible for third-party review.

510(k) Clearances

48 matches
K Number
Device Name
turbodent touch
BETA-POWDER
RONDOFLEX PLUS 360
PROSMILE AIR POLISHER AND PROPHYLAXIS POWDER
PREPAIR
VELOPEX AQUACUT FLUID ABRASION UNIT
GROMAN PREPMASTER
CLINPRO PROPHY POWDER
NEW PROPHY POWDER
JETSTREAM
JETPOLISHER
JETSONIC 2000
MINIBLASTER
DISPO ETCH
DISPODRILL
DISPOPROPHY
DENTO-PREP PARTICLE MICROBLASTER
KAVO CORUND HANDPIECE 2013
MACH 7
AIRDENT II CS
SIMPLEX AIRBRATOR (SAB-7)
S.S. WHITE TECHNOLOGIES, MODELS 6500-D,6500-E, AND 6500-F
JETSONIC 2000
AIR TECHNIQUES' AIRDENT II
PREPTECH(TM) 200 CAVITY PREPARATION SYSTEM
KREATIV MACH 5, MACH 5 PLUS, MACH M, MACH 6
AIRPREP SYSTEM - MODEL 9001
ULTRA-BLASTER
AEROETCHER
MICROETCHER AP
MICROJET CAVITY PREPARATION SYSTEM
ACCU-PREP
SIMPLEX AIRBRATOR
ABRADENT MICRO ABRASIVE SANDBLASTER MODEL DV-1
MICADENT
OPTIBLAST INTRAORAL SANDBLASTER
JETSTREAM CAVITY PREPARATION SYSTEM
SANDBLASTER
KREATIV MODEL KV-1
MICROPREP CAVITY PREPERATION SYSTEM
MODEL 2000 DENTAL AIR ABRASIVE SYSTEM
YOUNG PROPHY SYSTEM, PS UNIT
MICROETCHER
JETPOLISHER(TM)
D-23 DENTURE ADHESIVE
SCHEIN AP-1 AIR POLISHING UNIT
SATLEC PROPHY UNIT PU 3055
FIBER HEMOFILTERS FH55-FH77 & 88

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

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