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: EHD FDA class 2

Unit, X-Ray, Extraoral With Timer

Dental

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The Extraoral X-Ray Unit with Timer is a dental imaging system used to capture panoramic, cephalometric, or other extraoral radiographic views of the jaws, skull, and surrounding structures, with an integrated timer to control exposure duration. It is classified as FDA Class 2 (moderate risk), requiring 510(k) premarket clearance and compliance with special controls. The product code is EHD, regulated under 21 CFR 872.1800 in the Dental (DE) specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
Rextar Pro
XERO-alpha
WERAY
LifeRay Intraoral Handheld X-ray System
REMEX-GR100
XVbeam2000
Portable Dental X-Ray (AXR60 S); Portable Dental X-Ray (AXR65 S)
x-mind dc (under trademark Acteon), Owandy-RX DC (under trademark OwandyRadiology)
DVAS (DVAS-M, DVAS-W)
N1
HyperLight Portable X-ray Unit
Portable X-ray System Model Ray98(P)
Lumos 3DX
DHX-70H, XTG-70H
Portable X-ray System
Ai Ray Dental X-Ray Device
EzRay Air 2 Wall (Model: VEX-S350W)
Hybrid C70
FONA XDC
CLAROX
DT-703
HYBRID S70
ERI Handheld Dental X-ray System (Model AG100)
Portray
Portable Dental X-ray (NR-F350, CS 2400P, CS 2300P, R2 Port-X)
EzRay Air Portable (Model: VEX-P300)
Xcam
EZER, Portable X-ray System
MINE
Star-X, Intraoral X-ray System
RiX70 DC
Portable X-ray System (Model: MiniX-V, Mini X-S)
MobileX Portable X-ray System
Portable X-ray System
PORT-X IV
KaVo NOMAD Pro 2 Handheld X-ray System
Intraskan DC Plus
EzRay Air W
RX DC
EzRay Air (Model VEX-P300)
BI IMAGE-X EVOLUTION
Portable X-ray System (Model: MINIX-V / MINIX-S)
PHOT-X IIS MODEL 505
PORTABLE X-RAY SYSTEM (MODEL:EXARO,XRAY2GO)
X-MIND UNITY
ENDOGRAPH DC
REXTAR X
PORTABLE X-RAY SYSTEM
REXTAR, REXTAR LCD
VEX-S 100W INTRAORAL X-RAY SYSTEM

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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