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: ESI FDA class 3

Polymer, Natural-Absorbable Gelatin Material

Unknown

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The natural-absorbable gelatin material polymer is a bioabsorbable material derived from gelatin, intended for use in surgical procedures where a temporary support or hemostatic material that dissolves in tissue is required. It is classified as FDA Class 3, the highest risk category, requiring Premarket Approval (PMA) to demonstrate safety and effectiveness. The product code is ESI, reviewed by the Ear, Nose, Throat panel; no regulation number or formal medical specialty description is on record. No implant or life-sustaining flags apply.

510(k) Clearances

2 matches
K Number
Device Name
GASTROTEC
LM-150HT LIGHT SOURCE

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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