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: HKI FDA class 2

Camera, Ophthalmic, Ac-Powered

Ophthalmic

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The AC-Powered Ophthalmic Camera is an imaging device used to capture photographs or video of ocular structures, including the fundus, anterior segment, or external eye, for documentation, diagnosis, and monitoring of eye conditions. It is classified as FDA Class 2, indicating moderate risk, and requires 510(k) premarket clearance before marketing in the United States. The product code is HKI, regulated under 21 CFR 886.1120, within the Ophthalmic medical specialty. This device is eligible for third-party 510(k) review by an FDA-accredited reviewer.

510(k) Clearances

50+ matches
K Number
Device Name
Resolve Fundus Camera
Sentinel Camera
Verily Numetric Retinal Camera
CANON Fundus Camera CR-10 (CR-10)
Optina-4C (MHRC-C1N)
Zilia Ocular FC (ZIL-10002)
Phoenix ICON, Phoenix ICON GO
iExaminer System with Panoptic Plus
Eyer Retinal Camera NM-STD
Non-Mydriatic Retinal Camera NW500
RetCam Envision
NFC-600 Automated Portable Retinal Camera
Fundus Camera
VX650
Optomed Smartscope M5 with Optomed Smartscope FA
Canon non-mydriatic retinal camera CR series
XyCAM RI, XyCAM RI System, XyCAM Retinal Imaging System
Mydriatic Hyperspectral Retinal Camera (MHRC-C1)
Fundus Camera
KOWA nonmyd 8
KOWA DR-1a
Microperimeter MP-3, Microperimeter MP-3 Type S
NFC-700 non-mydriatic auto fundus camera
3nethra neo
LipiScan Dynamic Meibomian Imager
RetCam 3 ; RetCam Shuttle ; RetCam Portable
RetiCapture
Nexy
Optomed Aurora Camera with Aurora Retinal Module and Aurora Anterior Module
Phoenix Clinical ICON
HAAG-STREIT FUNDUS MODULE 300
Eyenez Ophthalmic Camera
MICROPERIMETER MP-3
LSFG-NAVI
LipiView II Ocular Surface Interferometer
TRC-NW8F PLUS NON-MYDRIATIC RETINAL CAMERA
TRC-NW400 NON-MYDRIATIC RETINAL CAMERA
COBRA FUNDUS CAMERA
KEELER KAPTURE SOFTWARE
OPTOMED SMARTSCOPE M5 / OPTOMED SMARTSCOPE EY4 / OPTOMED SMARTSCOPE ES2
IFUSION
TRC-50DX RETINAL CAMERA
TRC-NW8 NON-MYDRIATIC RETINAL CAMERA
DIGITAL RETINAL CAMERA
TRC-NW300 NON-MYDRIATIC RETINAL CAMERA
ICAM FUNDUS CAMERA
LIPIVIEW OCULAR SURFACE INTERFEROMETER
PANOPTIC
DIGITAL EYE-FUNDUS CAMERA
NON-MYDRIATIC AUTO FUNDUS CAMERA AFC-330 WITH IMAGE FILING SOFTWARE NA VIS-EX

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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