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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: OCO FDA unclassified

Mouthguard, Migraine/Tension Headache

Unknown

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The Migraine/Tension Headache Mouthguard (product code OCO) is a dental device used prophylactically for the treatment of medically diagnosed migraine pain and migraine-associated tension-type headaches by reducing trigeminally innervated muscular activity; it is also indicated for the prevention of bruxism and TMJ syndrome. The device works by mechanically reducing jaw muscle activity that contributes to headache and bruxing patterns. This device is FDA Unclassified (class U) with no assigned regulation number or medical specialty, pending classification, with an unclassified reason code indicating ongoing review. It carries no implant or life-sustaining flags.

510(k) Clearances

3 matches
K Number
Device Name
TMJ Relax
The Luco Hybrid OSA Appliance
NTI TENSION SUPPRESSION SYSTEM

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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