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: ESD FDA class 1

Hearing Aid, Air-Conduction, Prescription

Ear, Nose, Throat

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The prescription air-conduction hearing aid is a wearable sound-amplifying device intended to compensate for impaired hearing by conducting amplified sound to the ear through the air; it is dispensed by prescription. It is classified as FDA Class 1, the lowest regulatory risk, subject only to general controls and no premarket submission requirement. The product code is ESD, regulated under 21 CFR 874.3300 in the Ear, Nose, Throat specialty. No implant, life-sustaining, GMP-exempt, or third-party review designations apply.

510(k) Clearances

50+ matches
K Number
Device Name
Lyric4 Hearing Aid
LYRIC2
LYRIC HEARING AID
INSOUND XT SERIES HEARING AID
TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION)
SONIC INNOVATIONS COMPLETELY-IN-THE-CANAL DSP HEARING AID WITH SOFT SHELL
TRANQUIL TRI-OE, TRANQUIL TRI-COE, TRANQUIL TRI-CIC
ARGOSY PROGRAMMABLE ONQUE
SONIX HEARING AID FITTING AND PROGRAMMING SYSTEM
OPUS 2 - FULL CONCHA SERIES - ITE
OPUS 2 - COMPLETELY-IN-CANAL SERIES (CIC)
OPUS 2 - CANAL SERIES (ITC)
HI-69E, HI-69N, HI-69P
RESOUND DIGITAL 2000-BT W/DIGITAL 2000-DF (DIGITAL PROGRAMMER)
UNITRON MODEL SOUND F/XD PROGRAMMABLE
UNITRON MODEL SOUND F/XP PROGRAMMABLE MINI BTE
UNITRON MODEL F/X PROGRAMMABLE (MINI BTE)
RESOUND STEALTH CIC
HYUNJAE CORPORATION - NUSIL EARMOLD IMPRESSION MATERIAL
FUTURA 67M, 68M, MEGAPOWERMP97, INTEGRA 70,71,72,73, SUPRA 51,52, SUPRA 56,57,58,59, SUPREMA 45, 46, 47,48
MAGNATONE / STERLING/ ST; MAGNATONE/DB; MAGNATONE/ LIBERTY/ LB; MAGNATONE/ PEARL/PH C.I.C., S.P.I., ONE TOUCH, DESIGNER
PERFECT EAR/ MINI-CANAL/ PE-M, PE-ML, PE-MD), PERFECT EAR/ C.I.C./ (PEC, PE-CD) (WITH OR WITHOUT RID-WAX BARRIER)
OTICON DIGISOUND COMPACT
OTICON DIGISOUND ITE
AIR CONDUCTION HEARING AID
AM SERIES HEARING AID
DUALINE 100 BTE
MODEL C-1 HEARING AID
D72 DIGITAL
LORI/LORI, LORI-S (LORI STOCK AID)
Z DEQ-II
DRY & STORE
PRISMA
NEW SOUND HIDDEN AID COMPLETELY IN CANAL (CIC)
AIR CONDUCTION HAEARING AIDS
PHONAK NOVO FORTE E3
HEARTLAND TECHNOLOGIES, ITE, ITC, CIC
LORIPRO, LORIPRO II
IN THE EAR, IN THE CANAL, COMPLETELY IN THE CANAL
V-12 LONG LIFE 675 HEARING AID
PHONAK EPICA
AUDIFON H24 AGC/AUDIFON H25 AGC/AUDIFON H30 AGC
AUDIFON H20 PC/AUDIFON H32 PP
PHONAK MICROZOOM P 2
OVATION HDP
BETTER HEARING, INC. MODEL L-1 HEARING AID
JAZZ PP AGC-O, JAZZ PP
DAHLBERG/MIRACLE-EAR
MIRACLE-EAR ITE DIGITAL
TWIST PPAGC-1, TWIST PP

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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