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: EFT FDA class 1

Cleanser, Denture, Over The Counter

Dental

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The Over-the-Counter Denture Cleanser is a consumer dental product used to remove stains, plaque, bacteria, and food deposits from removable dentures through chemical or mechanical action, typically in the form of tablets, powders, or solutions used in soaking. It is classified as FDA Class 1, the lowest risk category, subject only to general controls and no premarket submission is required. The product code is EFT and the applicable regulation is 21 CFR 872.3520, under the Dental medical specialty.

510(k) Clearances

26 matches
K Number
Device Name
CLEANSE.FRESHEN.GO; ALIGNER CLEANSING TOWELETTE AND DENTAL APPLIANCE CLEANSER
MEDICAL INTERPOROUS
TRUBYTE DENTURE CLEANSER/POLISHING COMPOUND
OTC DENTURE CLEANSER
PROFAST(R)-DENTURE CLEANSER
DENTURE PRODUCT X
CFR MONOGRAPH
DENTURE DYNAMIC'S DENTURE MAGIC
ARGILITE 4 GOLD ALLOY FOR PORCELAIN
ORAD TOOTHBRUSH CLEANER
DENTCLEAN CONCENTRATED DENTURE CLEANSER
CLEAN DENT
EFFERVESCENT DENTURE CLEANSER
TATUNG'S DENTURE CLEANING SOLUTION
DENTURE CLEANSING TABLET
DENCLENZ
SUNBEAM ULTRASONIC DENTURE CLEANER MODEL 4220
TEEN CLEAN, RETAINER CLEANER
PEPSODENT DENTURE CLEANSER-WESTONE FORMULA
PEPSODENT DENTURE CLEANSER PDP FORMULA
PRE-KLENE ENAMEL CLEANER
DENTURE CLEANSER
SPRYCE, DENTURE CLEANSER
DENTURE CLEANER
DUO TWO LAYER DENTURE CLEANSER
ULTRASONIC DENTURE CLEANER

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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