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.

Let the assistant find your predicates

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

Free to try · every answer cites its records

Product Code: EYF FDA class 1

Protector, Wound, Plastic

General, Plastic Surgery

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The plastic wound protector is a device placed at a surgical incision to retract and protect the wound edges from contamination and mechanical trauma during abdominal or thoracic surgery, reducing the risk of wound infection and facilitating access. It is classified as FDA Class 1, indicating minimal risk, and requires 510(k) premarket clearance despite its Class 1 designation due to the submission type. The product code is EYF, regulated under 21 CFR 878.4014 in the General, Plastic Surgery specialty. No implant, life-sustaining, GMP-exempt, or third-party review designations apply.

510(k) Clearances

5 matches
K Number
Device Name
IRRIVAGE
HARDING STERNAL SHIELD
ANTI-FOG DISPOSABLE IV INDUCTION COVER
SI-PRO
COMFEEL PROTECTIVE RINGS

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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