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: MUW FDA class 2

Lens, Contact (Orthokeratology)

Ophthalmic

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An Orthokeratology Contact Lens is a rigid gas-permeable contact lens specifically designed and fitted to temporarily reshape the corneal surface overnight, reducing or eliminating refractive errors such as myopia so that patients can see clearly during the day without glasses or contact lenses. It is FDA Class 2, requiring 510(k) clearance, with product code MUW under 21 CFR 886.5916 in the Ophthalmic specialty. The device is not an implant and is not life-sustaining.

510(k) Clearances

6 matches
K Number
Device Name
iSee (roflufocon D, roflufocon E) Daily Wear Orthokeratology Contact Lenses
OPTIMUM GP OK Daily Wear Contact Lens (roflufocon D & E)
FLUOROPERM 151-OK, PARAGON HDS 100-OK
BOSTON EQUALENS II (OPRIFOCON A) CONTACT LENS FOR ORTHOKERATOLGY
FLUROPERM 60-OK, PARAGON HDS-OK
AIRPERM (SIFLUFOCON A) RIGID GAS PERMEABLE OK CONTACT LENSES FOR DAILY WEAR ORTHOKERATOLOGY

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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