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: LXM FDA unclassified

Manipulator, Plunger-Like Joint

Unknown

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The Plunger-Like Joint Manipulator (product code LXM) is a physical medicine device used to apply controlled force to joints for manipulative therapy, typically in chiropractic or osteopathic practice. It is currently unclassified (Class U) with no assigned regulation number or formal medical specialty, and is reviewed under the Physical Medicine (PM) panel. As an unclassified device, its regulatory status has not been fully determined. It is not flagged as an implant or life-sustaining device.

510(k) Clearances

32 matches
K Number
Device Name
SONIK MONARK 100
Spinalytics
Atlas Percussion Adjusting Instrument
VSTAAR AdjusteR
KHAN KINETIC TREATMENT (KKT-M2)
ACTIVATOR V-E
MAX ADJUSTING INSTRUMENT
IMPULSE IQ ADJUSTING INSTRUMENT
ACTIVATOR V SPINAL ADJUSTING INSTRUMENT
KHAN KINETIC TREATMENT DEVICE (KKT-M1)
TECHNOLOGY-ASSISTED MICRO-MOBILIZATION AND REFLEX STIMULATOR (TAMARS)
IMPULSE-ADJUSTING INSTRUMENT, CBP ADJUSTING INSTRUMENT, NEUROMECHANICAL ADJUSTING INSTRUMENT, MODELS 2003
FRYE ADJUSTING INSTRUMENT
HARRISON HAND HELD ADJUSTING INSTRUMENT
FS ACTIVATOR III
TORQUE INSTRUMENT, MODEL 8500
SENSE TECHNOLOGY INC. FRAS, SENSE TECHNOLOGY INC. PULSTAR
JTECH ADJUSTER REFLEX GUN
ACTIVATOR II
SMART ADJUSTER (SA201)
INTEGRATOR
HAND HELD ATLAS INSTRUMENT
ATLAS ORTHOGONAL PERCUSSION INSTTUMENT
MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENT
NEW-STIM SPINAL ADJUSTMENT INSTRUMENT
FORCE RECORDING AND ANALYSIS SYSTEM, MODEL 01
ARTHROSTIM MANIPULATOR
KINETIC TECHNOLOGY PRECISION ADJUSTOR MOD. SHLCP-5
KINETIC TECHNOLOGY PRECISION ADUSTOR MODEL SHLCP-4
KINETIC TECHNOLOGY POCKET PRECISION ADJUSTOR
KINETIC TECHNOOGY PRECISION ADJUSTOR MODEL SHLCP-1
PRECISION SPINAL ADJUSTER MODEL 115

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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