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: ION FDA class 1

Exerciser, Non-Measuring

Physical Medicine

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A Non-Measuring Exerciser is a Physical Medicine rehabilitation device designed to provide therapeutic exercise resistance or range-of-motion training without instrumentation to measure or display exercise parameters, such as basic resistance bands, springs, or simple exercise devices used in therapeutic settings. 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 ION, regulated under 21 CFR 890.5370, 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

43 matches
K Number
Device Name
ABLE-X
STANDEX
GRAVITY KING (DEEMED SE 87/09/18)
MOBILIZER
KNEE WALKER
FITNESS
PEDAL EXERCISER
ADJUST. WEIGHTS-BK5171-05,10,20 BEOK
DELUXE ADJUST-ANGLE BOARD-BK4066
GIREX
MADDATRAINER HAND EXERCISER
EXERCISER, PASSIVE, NON MEASURING
BACK ON TRACK INVERSION THERAPY & EXER
INFLATABLE HEAVY PLASTIC EXERCISER
PROGRESSIVE RESISTANCE EXERCISE CUFF
PLASTIC ELASTOMER ENCASED IN TERRY CLOTH
PLASTIC ELASTOMER IN CUBE FORM EXERCISE
PHYSICAL MEDICINE & REHABILITATION EQUIP
VISCO HANDEX-VARIOUS MODELS
BK-5305 MULTIPLE HAND GRID
MODELING COMPOUND AND FOAM EXERCISER
BACK RIE
BABY WALKER W/TOY CHEST
NON-MEASURING EXERCISERS
NON-MEASURING EXERCISERS
BK-5315-01 FOAM HAND EXERCISER, SMALL
FINGER, HAND & WRIST EXERCISER
THE VARIABLE LOAD KENETIC ENERGIZER
COLOR CODED PUTTY SOFT, REGULAR & FIRM
LOUNGE, TILT-A-BODY STRETCH
PUSH BALL INCLINE
VISA-GRIP
OBJECTS PRECISION HANDLING TEST KIT
FINGER EXERCISE BOARD
EXERCISER, LEG, LOWER EXTREMITY
EXERCISER, EXTENSOR WAND
RHEUMATOID HAND GYM
4-BAR KNEE-SHIN SET-UP
FLEXION-BRAKING KNEE-SHIN ASSEMBLY
SPIN-A-PULL
SHORT INFLATED ROLLS
CANOPY, PARACHUTE, BK-8110
BALLOONS, BK-8112, 8114

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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