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.
Polymer, Ent Synthetic-Pife, Silicon Elastomer, Polyethylene, Polyurethane
Ear, Nose, Throat
The ENT synthetic polymer (comprising PTFE, silicone elastomer, polyethylene, or polyurethane) is an implantable material used in reconstructive procedures of the ear, nose, and throat, such as ossicular reconstruction or tympanic membrane repair. It is classified as FDA Class 2, indicating moderate risk and requiring 510(k) premarket clearance. The product code is ESH, regulated under 21 CFR 874.3620 in the Ear, Nose, Throat specialty. This device is designated as an implant.
510(k) Clearances
1 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.