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: HQY FDA class 1

Sunglasses (Non-Prescription Including Photosensitive)

Ophthalmic

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Non-Prescription Sunglasses (Including Photosensitive) are ophthalmic protective eyewear designed to reduce ocular exposure to sunlight and ultraviolet radiation, including photochromic lenses that darken automatically in response to light intensity. These devices are FDA Class 1 (lowest risk), subject to general controls only without requiring premarket notification or approval. They carry product code HQY and are regulated under 21 CFR 886.5850, within the Ophthalmic medical specialty.

510(k) Clearances

50+ matches
K Number
Device Name
NON-PRESCRIPTION SUNGLASSES
NON-PRESCRIPTION SUNGLASSES
NON-PRESCRIPTION SUNGLASSES
SUNGLASSES
SUNGLASSES
MULTI
SUNGLASSES
NON-PRESCRIPTION SUNGLASSES
VENNETO
SUNGLASSES
SUNGLASSES
SUNGLASSES
SUNGLASSES (NON-PRESCRIPTION)
NORMA KAMLALI/ALFRED SUNG/ROOTS OF CANADA/STEEL MAXX SUNGLASS
SUNGLASSES
RUFF WORK EYEGEAR
NEVADA EYEWORKS, LUIGI LANATTA SUNGLASSES
D'ARC EYE CARE SUNGLASSES
MOMO DESIGN OR MOMO
SUNGLASSES
FOVS, BRILLARTE, ETC...
(BRAND NAME)
SUNGLASSES
SPECTACLE FRAMES (NON-PRESCRIPTION)
RIVIERA SUNGLASS4ES
CEBE
SUNGLASSES (NON-PRESCRIPTION)
SUNGLASSES (NON-PRESCRIPTION)
SUNGLASSES (FRAME,CELLULOSE PROPINATE, LENS, ACRYLIC)
OPTIM-EYES 450
GLARE WARE
DUQIAO
PATHFINDER SUNGLASSES
SUNGLASSES
AURORA SUNGLASSES,SKI GOGGLES AND PROTECTIVE/SAFTEY GOGGLES
UNIKA
GOLDEN STATE IMPORTS INTERNATIONAL, INC./ COLEMAN
CUSTOM OPTICAL SUNGLASS FRAMES
ARROW COMPANY
CLASSIC MATCH
LAXIMA INTERNATIONAL LIMITED SUNGLASSES
HWA MAO OPTICAL SUNGLASSES (NON-PRESCRIPTION)
EVEREST SUNGLASSES
SOLAR SPECS
BARAKKA, INFERNO, STERLING, AND/OR ONE
STYLE EYES OPTICS
VICTORY EYEWEAR CO
DAKOTA SMITH, NICOLE MILLER SUNGLASSES
ROCCOBAROCCO & PRO-DYNAMIX
JAMES ALEX SUNGLASSES

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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