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: OTZ FDA class 1

Graft Insertion Instrument For Endothelial Keratoplasty

Ophthalmic

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The Graft Insertion Instrument for Endothelial Keratoplasty (product code OTZ) is an ophthalmic surgical instrument inserted into the eye during keratoplasty surgery to direct the insertion of a corneal graft and then removed after insertion is completed. It is used in endothelial keratoplasty procedures such as DSEK or DMEK to facilitate precise delivery of donor corneal tissue. As an FDA Class 1 device under regulation 886.4300, it is subject only to general controls, the lowest FDA regulatory tier. It falls within the Ophthalmic specialty and is not an implant or life-sustaining device.

510(k) Clearances

5 matches
K Number
Device Name
EndoSerter-PL
EK DELIVERY DEVICE
NCI SPATULA
TRIMOTION INJECTOR
ENDOSERTER

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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