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: ECI FDA class 1

Band, Elastic, Orthodontic

Dental

View full classification →

The Elastic Orthodontic Band is a small, stretchable ring placed around individual teeth or used between brackets to apply light, continuous forces that assist in tooth movement and space closure during 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 ECI and the applicable regulation is 21 CFR 872.5410, under the Dental medical specialty.

510(k) Clearances

25 matches
K Number
Device Name
POWER COINS GLOW IN THE DARK LIGATURES
GLENROE CHAIN
GLENROE GLOW IN DARK ELASTOMERIC LIGATURES
ORTHODONTIC ELASTOMERIC LAGATURE MODULE
ORTHODONTIC ELASTOMERIC CHAIN
ORTHODONTIC ELASTOMERIC SEPARATOR MODULE
ORTHODONTIC ELASTOMERIC TUBE/THREAD
ALASTIK
PRO'S NEO-LASTICS
DENTAURUM OLYMPIA LATEX-ELASTICS AND DENTAURUM LATEX-ELASTICS
ORTHODONTIC ELASTOMER
GLENROE CHAIN
ALASTIK NS
SINGLES
TUFF TIES
GLENROE ORTHO SEPS
UNI-STICK PLASTIC LIGATURE, MODIFIED
RUBBER BAND, STERILE
A-COMPANY SEPARATING ELASTICS
A-COMPANY ELASTIC LIGATURE RINGS
A-COMPANY ELASTIC ROTATION WEDGES
A-COMPANY ELASTOMERIC CHAIN DISPENSER
A-COMPANY ELASTOMERIC TUBING
ORTHODONTIC ELASTICS
HYGIENIC ANCHORINGS

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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