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.

Product Code: HXW FDA class 1

Bender

Orthopedic

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An orthopedic bender is a handheld instrument used to bend fixation rods, plates, wires, or other metallic hardware to the desired angle or curvature to match patient anatomy during surgical implantation. It is classified as an FDA Class 1 device under 21 CFR 888.4540, indicating minimal risk and general controls only. Product code HXW falls under the Orthopedic medical specialty.

510(k) Clearances

3 matches
K Number
Device Name
ACROMED BONE PLATE BENDER
DRIVER-BENDER-EXTRACTOR, BONE PIN
RD 140 SURGICAL BENDER

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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