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: NHN FDA class 2

Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy

Physical Medicine

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The Powered Light Based Laser Non-Thermal Instrument With Non-Heating Photon Energy (product code NHN) is a physical medicine device that uses low-level laser or light energy in a non-thermal manner to deliver photon energy to tissue for therapeutic effects, as described in its definition. It is classified as an FDA Class 2 device within the Physical Medicine specialty, requiring 510(k) premarket clearance. No specific regulation number has been assigned to this product code. The device is not flagged as an implant or life-sustaining device.

510(k) Clearances

50+ matches
K Number
Device Name
Enhanced Handheld Pain Relief Laser Instrument (GD-P-E)
Therapy EC, Therapy XT
Erchonia FX-405
FibroLux
Erchonia GVL
PainTB, PainTJ
Erchonia FX-405
Erchonia XLR8
Erchonia EVRL
Erchonia FX-635
Erchonia FX-635
Collagentex Rx-6
MR4 Laser
Collagentex Rx-1
Erchonia EVRL
Erchonia PL Touch
TLC-2000 Therapeutic Medical Laser System
ERCHONIA ALLAY
ERCHONIA EMERGE
ERCHONIA PL5000
MLS-AC DERMA SCANNER
THL1 LASER
LIGHTSTREAM LOW LEVEL LASER
QLASER SYSTEM
LEP2000 THERAPY SYSTEM
ERCHONIA EML LASER
LD-I 75 AND LD-I 200
LUMINEX LL LASER SYSTEM
ELITE ELECTROMED L.I.T.E. 4/1
GRT LITE, MODEL 8-A
EXCALIBUR IV LIGHT THERAPY SYSTEM, MODEL SGEX4-001
THERALASE TLC-1000 THERAPEUTIC MEDICAL LASER SYSTEM
OMEGA EXCEL/XP LASER SYSTEM
LAZRPULSR 4X
LAPEX 2000
EXCALIBUR LIGHT THERAPY SYSTEM, MODEL SGIEX-04-001
ERCHONIA EML LASER
QUANTUM LIGHT THERAPY SYSTEM
ACCULASER PRO4
BIOPTRON PRO LIGHT THERAPY SYSTEM AND BIOPTRON COMPACT III LIGHT THERAPY SYSTEM
AXIOM BIOLASER LLLT SERIES-3
DIOBEAM 830
AXIOM BIOLASER LLLT SERIES-1
POWER LASER 90
NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORY
THOR DDII 830CL3 LASER SYSTEM
TRILUMINA THERAPEUTIC LASER SYSTEM
MEDX LCS LASER SERIES
ACCULASER PRO LOW LEVEL LASER THERAPY DEVICE
MICROLIGHT 830 LASER 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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