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: DZC FDA class 1

Wire, Orthodontic

Dental

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The Orthodontic Wire is a dental device made from metal alloy formed into an arch shape and seated in orthodontic brackets to apply continuous forces that guide tooth movement over the course of orthodontic treatment. 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 DZC and the applicable regulation is 21 CFR 872.5410, under the Dental medical specialty.

510(k) Clearances

30 matches
K Number
Device Name
HYPERELASTIC WIRE
HAWLEY RETAINER ORTHODONTIC APPLICANCE KIT
NITINOL, NITI
DENTAURUM STEEL LIGATURE WIRES
DENTAURUM WIRES
FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE
NITI COIL SPRINGS
STAINLESS STEEL ARCHES REPACKER RELABETER
REVERSE SURVE NITI ARCH WIRE
REVERSE CURVE NITI ARCH WIRE REPACKER RELABETER
NITI ARCH WIRE ON A SPOOL
STAINLESS STEEL ARCHES
COATED ORTHODONTIC DEVICES
TITAN SEPARATING SPRING
ORTHODONTIC ARCH WIRE
DIMPLED MULTI MODULUS ARCH WIRE
.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING
THE ULTIMATE RCS ARCH WIRE
BIOFORCE WIRE
NITINOL GENTLE TOUCH COIL SPRING
GAC THUMB-SUCKING CONTROL APPLIANCE
FLEXMEDICS NITINOL ARCH WIRE
INTERPORE 200 POROUS HYDROXYAPATITE
A COMPANY BRASS SEPARATING RINGS
SENTINOL -ORTHODONTIC ARCH WIRE
FILAFEX TM, ESTHETIC ORTHODONTIC WIRE
ORTHODONTIC WIRE
ALINE ORTHODONTIC ARCHWIRE
FILAFEX ESTHETIC ORTHODINIC WIRE
PAC-AID

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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