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.
Instrument, Measuring, Corneal Radius
Ophthalmic
The Corneal Radius Measuring Instrument is an ophthalmic device used to quantify the curvature of the cornea, providing measurements essential for contact lens fitting, keratoconus monitoring, and pre-surgical corneal assessment. It is classified as FDA Class 1, meaning it presents the lowest level of risk and requires only general controls such as proper labeling and establishment registration. The product code is HJB, regulated under 21 CFR 886.1450, within the Ophthalmic medical specialty. No special risk flags apply to this device.
510(k) Clearances
5 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.