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: ELC FDA class 2

Scaler, Ultrasonic

Dental

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The Ultrasonic Scaler is a dental device that uses high-frequency ultrasonic vibrations transmitted through a metal tip or insert to remove calculus, biofilm, and stain from tooth surfaces and within periodontal pockets, often combined with a water lavage for cooling and debris removal. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket clearance. The product code is ELC, regulated under 21 CFR 872.4850 in the Dental (DE) specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
Integrated Endo System (Meet Endo-II)
OdneClean
Ultrasonic Scaler (WD-JY-B002,WD-JY-W001,WD-JY-R003,WD-JY-G004,WD-JY-B003,WD-JY-C006,WD-JY-M0014, WD-JY-N0015,WD-JY-N0016,WD-JY-N0017,WD-JY-E007, WD-JY-F008,WD-JY-A005,WD-JY-H009,WD-JY-I0011, WD-JY-K0012,WD-JY-K0013,WD-JY-K0014, WD-JY-L0013,WD-JY-L0014,WD-JY-L0015, WD-JY-L0016,WD-JY-L0017)
BioSonic US200 Ultrasonic Scaler (60034537)
SP NEWTRON CAN-A; MODULE NEWTRON CAN-A EMB; SUPPORT XINETIC; NWT CAN SLIM LED CORD G3 SHORT; NWT CAN SLIM LED CORD G3 LONG
EDS Calculus Softener TURBO CR
Ultrasonic Scaler Tips
Proxeo ULTRA (PB-510, PB-520 and PB-530)
Combi Touch
Endo Ultrasonic Activator
Ultrasonic Endo Activation Device (Model:Actor I pro)
EVOCLEAN CLEANsert Ultrasonic Insert
Dental Scaler and Air Polisher
EndoPilot2
GentleWave X
TTBIO EVOCLEAN Ultrasonic Scaler
EMS AIRFLOW Prophylaxis Master, EMS AIRFLOW One
Piezon Built-in Kit, Piezon Built-in Kit LED
tün® ultrasonic tips product family
Sonendo GentleWave System
AW-100
COMPACT S, COMPACT S (LED)
Ultrasonic scaler
Y-MIC
Sonendo GentleWave System
Sonendo Gentle Wave System
COMPACT PIEZO LED
Cavitron Touch Ultrasonic Scaling System
Sonendo GentleWave System
ULTRASONIC SCALER
EMS PIEZON 707 BIK AND PIEZON 707 BIK LED
MULTIPIEZO PRO, MULTIPIEZO
SONENDO OMNICLEAN ENDOTHERPAY SYSTEM CONSOLE, SONENDO OMNICLEAN MOLAR PROCEDURE KIT
NEWTRON P5 XS B.LED
NEWTRON P5, NEWTRON P5 B.LED
EDS ULTRASONIC TIPS
ENDOCENTER
PIEZON 250
NEWTRON BOOSTER
PIEZON 150
R7
BIOSONIC SUVI PIEZEOELECTRIC SCALER AND POLISHER
AEU-525 TRANSPORT III PORTABLE DENTAL SYSTEM
CAVITRON PROPHY-JET AIR POLISHING PROPHYLAXIS SYSTEM
SONENDO ENDOTHERAPY SYSTEM
ENGLER 25K SERIES ULTRASONIC INSERTS
AEI DR. TERAUCHI ULTRASONIC TIPS
ADVANCED ENDODONTIC SYSTEM- DESIGNER SERIES
ULTRASONIC SCALER
ULTRASONIC SCALER

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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