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: HLM FDA class 1

Instrument, Measuring, Lens, Ac-Powered

Ophthalmic

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The AC-Powered Ophthalmic Lens Measuring Instrument is an electrically powered device, such as a lensometer or focimeter, used to measure the optical power and other properties of ophthalmic lenses including sphere, cylinder, axis, and prism. It is classified as FDA Class 1, the lowest risk category, subject only to general controls without any premarket notification requirement. The product code is HLM, regulated under 21 CFR 886.1425, within the Ophthalmic medical specialty. No special risk flags apply to this device.

510(k) Clearances

16 matches
K Number
Device Name
LENSCHEK
AL-3300
AUTOMATIC LENSOMETER
MARCO STANDARD LENSMETERS 101,201
MARCO LM-770 DIGITAL PROJECTION LENSMETER
BURTON RADIUSGAUGE - MODEL 2030
BURTON LENSMETER - MODEL 2021
BURTON LENSMETER
WOODLYN CLASSIC LENSMETER
NIDEK LM-870 AUTOMATIC LENSMETER
BAUSCH & LOMB VERTOMETER V-5
LM-850 AUTOMATIC LENSMETER
DIMENSION I REFRACTION SYSTEM
VERI-VU LENSOMETER
INSTRUMENTS, OVERREFRACTION SYSTEM
LENSOMETER MODEL 11

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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