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: JFA FDA class 1

Exerciser, Finger, Powered

Physical Medicine

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A Powered Finger Exerciser is a physical medicine device that uses motorized or powered mechanisms to repetitively move and rehabilitate the fingers, assisting patients recovering from hand injuries, surgeries, or neurological conditions affecting finger mobility. It is classified as FDA Class 1 (lowest risk), subject only to general controls. The product code is JFA, regulated under 21 CFR 890.5410, within the Physical Medicine medical specialty. No special flags apply to this device.

510(k) Clearances

12 matches
K Number
Device Name
THERMAFLEX, MODEL SD 55 C.P.M.H.
JACE MODEL H440 HAND CPM DEVICE
HAND THERAPY ASSOST
JACE MODEL PM-410 HAND CPM DEVICE
MOBILIMB H3 HAND CPM UNIT
DANNIFLEX CPM 880(TM)
TORONTO/MOBILIMB HAND C.P.M.
MOBILIMB HAND C.P.M. UNIT
ACE AIM - CPM HAND UNIT
MOBILIMB HAND UNIT
SUTTER CPM 5000
BURNETT-KETCHUM DYNAMIC HAND EXERCISER

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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