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: IOD FDA class 1

Components, Exercise

Physical Medicine

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Exercise Components are individual parts or accessories used in Physical Medicine rehabilitation exercise equipment, including resistance bands, pulleys, weights, handles, and mechanical components that form part of a therapeutic exercise apparatus used for strengthening and functional rehabilitation. It is classified as FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. The product code is IOD, regulated under 21 CFR 890.5350, within the Physical Medicine medical specialty. This device is GMP exempt, indicating it is not subject to full good manufacturing practice requirements.

510(k) Clearances

11 matches
K Number
Device Name
DELUXE TRACTION EXERCISE GLOVE BK5035
SURGICAL TUBING
ANKLE WEIGHTS
SOLID WOOD CONE
COLOR CODED WEIGHT CUFFS
THERAPY BENCH
CANVAS WEDGE
SANDBAGS, VARIOUS WEIGHTS
FLEXION MITTENS
HAND SCREW CLAMP
SHEET METAL CLAMP

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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