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.
File, Pulp Canal, Endodontic
Dental
The Endodontic Pulp Canal File is a fine, flexible hand instrument with a serrated or helically cut shaft used to enlarge and shape root canals by filing action against the canal walls, removing dentin to achieve the desired preparation geometry. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is EKS, regulated under 21 CFR 872.4565 in the Dental (DE) specialty.
510(k) Clearances
31 matchesWhat 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.