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: LXB FDA class 2

Hearing Aid, Bone Conduction

Ear, Nose, Throat

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The Bone Conduction Hearing Aid (product code LXB) is a hearing device that transmits sound vibrations through the bones of the skull to the cochlea, bypassing the outer and middle ear, and is used by individuals with conductive hearing loss or single-sided deafness. Regulated under 21 CFR 874.3302 and classified as a Class 2 device, it requires a 510(k) premarket notification and is eligible for third-party review. The device falls under the Ear, Nose, and Throat medical specialty. It is not an implant and is not life-sustaining.

510(k) Clearances

49 matches
K Number
Device Name
Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha Smart App (iOS) (P1646054); Baha Smart App (Android) (P1646035); Baha SoundBand
contact forte Alpha
Ponto 5 SuperPower
Cochlear Baha 6 System, Cochlear Baha Fitting Software 6, Cochlear Baha Baha Smart App
Ponto 5 Mini
Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App
Ponto 4
ADHEAR System
Cochlear Baha SoundArc
Ponto 3, Ponto 3 Power and Ponto 3 SuperPower
Sophono Bone Conduction Systems (S) Configuration and (M) Configuration
Baha 5 Power Sound Processor
Baha 5 Super Power Sound Processor
Cordelle II Sound Processor
Baha 5 Sound Processor
PONTO PLUS AND PONTO PLUS POWER
OTOMAG BONE CONDUCATION HEARING SYSTEM
COCHLEAR BAHA IMPLANT SYSTEM, COCHLEAR BAHA ATTRACT
COCHLEAR BAHA 4 SOUND PROCESSOR
OTOMAG BONE CONDUCTION HEARING SYSTEM
AN EVO 1, CS EVO 1, CONTACT MINI, APOLLON
SOUNDBITE HEARING SYSTEM BY SONITUS MEDICAL
PONTO PRO POWER
OTOMAG BONE CONDUCTION HEARING SYSTEM MODEL ALPHA 1 (S) AND ALPHA 1 (M)
BAHA 3 POWER SOUND PROCESSOR
SOUNDBITE HEARING SYSTEM BY SONITUS
BIA300 SERIES IMPLANT AND ABUTMENT, BI300 IMPLANT, BA300 ABUTMENT
OTOMAG BONE CONDUCTION HEARING SYSTEM
PONTO PRO
COCHLEAR BAHA BP100
OBC BONE ANCHORED HEARING AID SYSTEM
BAHA INTENSO
TRANSEAR BONE CONDUCTION HEARING AID
TRANSEAR BONE CONDUCTION HEARING AID
BAHA DIVINO
BRANENMARK BONE-ANCHORED-HEARING AID (BAHA)
BILATERAL FITTING OF THE BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM.
HEADBAND FOR BAHA
BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II
NOBELPHARMA BONE ANCHORED HEARING AID
SECOND EAR BONE CONDUCTION HEARING AID
HI SONIC 2000 DIGITAL HEARING INSTRUMENT
VIENNATONE AN, VIENNATONE AS FIDELITY F228, FIDELITY F229
MODIFIED IMPLANT FOR XOMED AUDIANT BONE CONDUCTOR
XOMED AUDIANT BONE CONDUCTOR
ADDITIONAL INDICATIONS FOR XOMED AUDIANT BONE CON.
XOMED AUDIANT BONE CONDUCTOR AT THE EAR SOUND PRO.
XOMED AUDIANT BONE CONDUCTOR W/IMPROVED AA COIL
AUDIANT BONE CONDUCTOR OR A.B.C.

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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