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: HJN FDA class 1

Transilluminator, Battery-Powered

Ophthalmic

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The Battery-Powered Ophthalmic Transilluminator is a portable, battery-operated light source used to illuminate ocular and periocular structures, helping clinicians detect abnormalities such as masses or fluid within the eye or orbit. It is classified as FDA Class 1, the lowest risk level, subject only to general controls without any premarket notification requirement. The product code is HJN, regulated under 21 CFR 886.1945, within the Ophthalmic medical specialty. No special risk flags apply to this device.

510(k) Clearances

3 matches
K Number
Device Name
VENOSCOPE
LULMITEX NEONATAL TRANSILLUMINATOR
SYLVAN PEDIASCAN 200 TRANSILLUMINATOR

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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