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: DZN FDA class 1

Instruments, Dental Hand

Dental

View full classification →

Dental Hand Instruments are a broad category of hand-held, non-powered tools used by dental clinicians for examining, scaling, probing, carving, and otherwise manipulating teeth and oral tissues during preventive and restorative dental procedures. They are classified as FDA Class 1, the lowest risk category, subject only to general controls and no premarket submission is required. The product code is DZN and the applicable regulation is 21 CFR 872.4565, under the Dental medical specialty.

510(k) Clearances

16 matches
K Number
Device Name
COMPOTHIXO
DENTAL MATRIX BAND
CONTACT MOLAR BANDS AND CONTOUR STRIPS
CENTRIX PCR MOLAR MATRIX FORMS (BANDS)
TIGER BAND
INTERDENTAL WEDGES
DENTAL MATRIX BAND
COLORED WEDGE USED TO SEPARATE TEETH
PALODENT MATRICES & BITINE RINGS
COREFORM MOLDS
HEMO-WEDGE
RUWA MATRIX STRIPS
HOWMEDICA STRIP CROWN
ACCOR MATRIX
MATRIX STRIP, DEAD-SOFT
WEDGES, RETAINING, MATRIX

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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