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: EAZ FDA class 1

Light, Operating, Dental

Dental

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The Dental Operating Light is a high-intensity light fixture positioned over the dental chair to provide focused, shadow-free illumination of the patient's oral cavity during dental 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 EAZ and the applicable regulation is 21 CFR 872.4630, under the Dental medical specialty.

510(k) Clearances

23 matches
K Number
Device Name
MICROLUX/BLU
MICROLUX DL
VIZILITE-BLUE ORAL EXAM KIT
SPECULITE/ORALLITE
DENTAL LIGHT
SIROLUX FANTASTIC
ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT
DELIGHT
MICRONAIRE ISO-HOOD MAX 5UV
MINIFLEX AND PERSONAL UNIT
DEFIANCE MODEL FUS 336
ISOLIGHT
A-DEC DENTAL LIGHT
DENTAL EQUIPMENT PROTECTION DEVICES
DENTAL LAMP HANDLE COVER
THE WOOG ORATEST
F-11 REFLECTOR / F-II STANDARD REFLECTOR
OPTI-BEAM IV
LUNA-VUE DENTAL OPERATING LIGHT
KLIP-LITE
DENTAL LIGHT
JOY LIGHT
RITTER STARLIGHT DENTAL OPERATING LIGHT

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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