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: EZR FDA class 1

Cement, Stomal Appliance, Ostomy

Gastroenterology, Urology

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The Stomal Appliance Cement for Ostomy (product code EZR) is an adhesive substance used to secure ostomy appliances, such as pouches or flanges, to the peristomal skin. It is an FDA Class 1 device (lowest risk), subject only to general controls with no 510(k) required. It is regulated under 21 CFR 876.5900 in the Gastroenterology and Urology specialty. No special flags apply.

510(k) Clearances

6 matches
K Number
Device Name
UNITED SKIN BARRIER PASTE
STOMAHESIVE PASTE PROTECTIVE SKIN BARR
COLO-TAPE
OSTOMY KARAYA GUM POWDER
KARAYA GUM POWDER
KARAYA GUM PRODUCTS - PROCESS CHANGE

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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