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.

Let the assistant find your predicates

Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

Free to try · every answer cites its records

Product Code: LRA FDA unclassified

Hearing Aid, Tactile

Unknown

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A tactile hearing aid is a device that converts sound signals into vibrotactile stimulation delivered to the skin surface, providing an alternative sensory channel for individuals with severe or profound hearing loss who cannot benefit from conventional acoustic hearing aids. This device is currently unclassified (Class U) by the FDA, meaning it has not been placed into a final regulatory classification category. The product code is LRA; no regulation number or medical specialty is on file for this entry. No special flags apply to this device.

510(k) Clearances

8 matches
K Number
Device Name
ETA
WEARABLE TWENTY-FOUR CHANNEL VIBROTACTILE VOCODER
TACTICON 1600
TEACHER TM
KANIEVSKI SENSORY AID OR DEVICE
TACTIL EAR
TACTAID
VIBRO-COM COMMUNICATOR #8827

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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