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: PHL FDA class 2

Powered Exoskeleton

Physical Medicine

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The Powered Exoskeleton is a prescription motorized orthotic device that is placed over a person's paralyzed or weakened lower extremity limb(s) to assist with mobility and rehabilitation for medical purposes. It is an FDA Class 2 device regulated under 21 CFR 890.3480, requiring 510(k) premarket notification, within the Physical Medicine (PM) specialty with Neurology (NE) panel review. The product code is PHL. This device is not an implant and is not life-sustaining.

510(k) Clearances

23 matches
K Number
Device Name
ReWalk® 7 Personal Exoskeleton (50-20-0005)
Medical HAL Lower Limb Type (HAL-ML)
Atalante X
ReWalk P6.0
Atalante
EksoNR
GEMS-H
ExoAtlet-II
HAL for Medical Use(Lower Limb type)
Keeogo Dermoskeleton System
EksoNR
ReWalk P6.0
ReWalk Restore
Phoenix
Honda Walking Assist Device
Indego(R)
HAL for Medical Use (Lower Limb Type)
Indego
ReWalk(TM)
Ekso™ (version 1.1) and Ekso GT™ (version 1.2)
Ekso™ (version 1.1) and Ekso GT™ (version 1.2)
Indego
REWALK

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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