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.

Let the assistant find your predicates

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

Free to try · every answer cites its records

Product Code: EAX FDA class 1

Mirror, Mouth

Dental

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The Mouth Mirror is a hand-held dental instrument with a small reflective head used by dental clinicians to gain indirect visualization of oral structures that cannot be directly seen, and to retract soft tissues during examination and 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 EAX and the applicable regulation is 21 CFR 872.4565, under the Dental medical specialty.

510(k) Clearances

12 matches
K Number
Device Name
ORALVUE DENTAL MIRROR
RANIR PLAX RX
RETRO MIRROR
NIL
DISPOSABLE MOUTH MIRRORS, SINGLE USE ONLY
GLASS MOUTH MIRRORS, REUSABLE
FOGCUTTER DENTAL MOUTH MIRROR
FIBERGLASS MOUTH MIRRORS
PERI MIRROR/SALIVA EJECTOR
ELECTRIC MOUTH MIRROR
BEACH MOUTH MIRROR
ORAVIEW BY WATER PIK

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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