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.

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Describe your device and the Research Assistant searches 510(k)s, compares intended use, and drafts a predicate shortlist — with citations.

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Product Code: MLP FDA class 2

Keratoprosthesis, Temporary Implant, Surgical Use

Ophthalmic

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The Temporary Implant Keratoprosthesis for Surgical Use is a temporary artificial cornea implanted intraocularly during vitreoretinal surgery to replace the patient's cornea when optical clarity is compromised, enabling surgical visualization of the posterior segment and then removed at the end of the procedure. Classified as a Class 2 implantable device under 21 CFR 886.3400 within the Ophthalmic specialty, it requires 510(k) premarket notification. It carries an implant flag due to its intraoperative intraocular placement.

510(k) Clearances

4 matches
K Number
Device Name
LANDERS WIDE FIELD TEMPORARY KERATOPROSTHESIS
ECKHARDT TEMPORARY KERATOPROSTHESIS
COBO TEMPORARY KERATOPROSTHESIS
LANDERS-FOULKS TEMP. KERATOPROSTHESIS

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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