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: IKZ FDA class 2

Bed, Patient Rotation, Powered

Physical Medicine

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A Powered Patient Rotation Bed is a motorized therapeutic bed used in Physical Medicine to continuously or intermittently rotate patients who are bedridden, used to prevent complications associated with immobility such as pressure ulcers, deep vein thrombosis, and pulmonary complications. It is classified as FDA Class 2, representing moderate risk, meaning it requires a 510(k) premarket notification demonstrating substantial equivalence to a predicate device before marketing. The product code is IKZ, regulated under 21 CFR 890.5225, within the Physical Medicine medical specialty.

510(k) Clearances

17 matches
K Number
Device Name
PRESSUREGUARD IV
RUMORS DYNAMIC AIR THERAPY UNIT
CLINIDYNE ROTATIONAL THERAPY MATTRESS SYSTEM
THE FREEDOM BED
PULMONEX DYNAMIC AIR THERAPY UNIT
MODEL TURN Q PLUS AUTOMATIC TURNING MATTRESS WITH LOW AIR LOSS THERAPY
THE CRADLE
OSCILLAIR 3000 LOW AIR LOSS KINETIC THERAPY BED
TURN EZ BED DEVICE
KUDO (POWERED ROTATION BED)
ROTO REST; TRAUMA AND INTENSIVE CARE BED
KEANE MOBILITY BED
EMERSON MOTION BED 6-MS & 6-ME
EGERTON TURNING & TILTING BED
KINETIC MOTION BED
ROTO REST KINETIC TREATMENT TABLE PEDIA
POWERED PATIENT SYSTEM

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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