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.

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

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Product Code: ONE FDA class 2

Powered Light Based Non-Laser Surgical Instrument

General, Plastic Surgery

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The Powered Light Based Non-Laser Surgical Instrument (product code ONE) is a Class 2 surgical device regulated under 21 CFR 878.4810 in the General, Plastic Surgery specialty (SU), cleared via 510(k). It is a non-laser light-based device typically indicated for general surgical purposes across specialties including general and plastic surgery, dermatology, podiatry, ENT, gynecology, neurosurgery, orthopedics, and dental/oral surgery. The device is eligible for third-party review and is not an implant or life-sustaining device.

510(k) Clearances

7 matches
K Number
Device Name
handLITE (TN19S)
Philips BlueControl
TANDA MAX
PLASMALUXLS
BABY QUASAR
CLEARWAVE PHOTOTHERAPY SYSTEM FOR ACNE, MODEL: CWST2
ANTI-WRINKLE (AGING) LIGHT, MODEL AAL

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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