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: LRB FDA class 1

Face Plate Hearing Aid

Ear, Nose, Throat

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A face plate hearing aid is a type of hearing aid configured with a faceplate housing, typically used with behind-the-ear or in-the-ear designs, which amplifies sound to assist individuals with hearing loss. It is classified as a Class 1 (lowest risk) device, subject only to general controls, representing the least burdensome regulatory category. The product code is LRB, regulated under 21 CFR 874.3300, within the Ear, Nose, and Throat medical specialty. No special flags apply to this device.

510(k) Clearances

24 matches
K Number
Device Name
FACEPLATE ASSEMBLY
INTRASTAR PRE-WIRED FACEPLATE FOR IN-THE-EAR HEARING AIDS
MODULE PROGRAM
AUDINA PREWIRES (FACEPLATE HEARING AID SERIES)
ARTISAN PROGRAMMER & HEARING AID
GOLD L MODULE, ITE
SILVER LD MODULE, ITE
SILVER L MODULE, ITE
SILVER PPP MODULE, ITE
GOLD CD MODULE, ITE
GOLD K AMP, ITE
GOLD AF MODULE, ITE
SILVER RECHARGEABLE MODULE, ITE
FACEPLATE ITE HEARING AID MODEL TCA
FACEPLATE ITE HEARING AID MODEL 28A
OVERSIGHT PROGRAM FOR IN-OFFICE ASSEMBLY, HRNG AID
OLYMPIA FACEPLATE MODULE
STARKEY MODEL P1 MODULE
AIR CONDUCTION IN-THE-EAR HEARING AID UA/115/SCR
SERVICE MASTER (IMPULSE)
IN THE EAR & IN THE CANAL HEARING AID FACE PLATE
FACEPLATE, CUSTOM IN-THE-EAR HEARING AID, FPR
FACEPLATE, CUSTOM IN-THE-EAR HEARING AID, MCA10
RELIABLE

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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