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: MNE FDA class 1

Orthosis, Moldable, Supportive, Skin Protective

Physical Medicine

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The Moldable Supportive Skin-Protective Orthosis is a custom-moldable or prefabricated orthopedic support device applied externally to the body to provide structural support, protect skin integrity, and maintain positioning in patients with musculoskeletal conditions, pressure injuries, or post-surgical needs. Classified as a Class 1 device under 21 CFR 890.3475 within the Physical Medicine specialty, it is subject to general controls only and is generally exempt from 510(k) premarket notification. It carries no implant or life-sustaining flags.

510(k) Clearances

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K Number
Device Name
PODIATRIC MATERIAL
PODIATRIC MATERIAL

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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