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: FSY FDA class 2

Light, Surgical, Ceiling Mounted

General, Plastic Surgery

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A ceiling-mounted surgical light is a fixed overhead lighting system installed in operating rooms to provide hands-free, overhead illumination of the surgical field from an adjustable ceiling mounting point. It is classified as FDA Class 2 (moderate risk), subject to general and special controls, and requires 510(k) premarket notification. The product code is FSY, regulated under 21 CFR 878.4580, within the General, Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

50+ matches
K Number
Device Name
Leo Minor
CLAVEGUARD FREEDOM SURGICAL LIGHT
MI-750 PROCEDURAL/MINOR SURGICAL LIGHT
ZF 720
VIDA LED SURGICAL LIGHTING SYSTEM, V SERIES
MACH LED 2SC
MACH LED 2MC
VISUM BLADE LED SURGICAL LIGHTING SYSTEM
VIDA LED SURGICAL LIGHTING SYSTEM
AMICO CE SERIES SURGICAL LIGHTS, MIRA LED SERIES MINOR SURGICAL LIGHTS
ORICARE L2700
CHROMOPHARE F 628 AND F 528
TRULIGHT 5520 AND TRULIGHT 5320
AIM 200, MAJOR SURGICAL LIGHT
STARTROL LED LIGHTING SYSTEMS (X=# OF PODS, Y=# OF LEDS, N=TO MOUNTING STYLE) MODEL X X Y -N-S-W. X=NUMBER OF LIGHT PODS
MACH LED MC
MACH LED SC
CHROMOPHARE E 668
NUVO VERDE LED LIGHTING SYSTEM
CHROMOPHARE E 778 AND E 558
CHROMOPHARE E-SERIES
HARMONY LED-1 SURGICAL LIGHTING SYSTEM
AURORA LED SERIES SURGICAL LIGHTS
POWERLED SURGICAL LIGHT SYSTEM
M3
ILED
VISUM LED SURGICAL LIGHTING SYSTEM
OUTPATIENT III MINOR SURGERY LIGHT
DUAL LED LITE ENGINE WITH ILLUMINATION LED CABLE COUPLED TO A LED LITE HEAD
ALM X'TEN (X10) SURGICAL LIGHT SYSTEM
MODIFICATION TO PRISMALIX SURGICAL LIGHT
STRYKER VISUM SURGICAL LIGHTING SYSTEM
CONMED INTEGRATED SYSTEMS NURSES ASSISTANT
AXCEL SURGICAL LIGHT
CHROMOPHARE X 65
STELLAR SERIES SURGICAL LIGHTS WITH HERMES
TRUMPF SURGICAL LIGHTS, MODELS 301,501,701,1001
VAL LUX 600 SURGICAL LIGHT (PLUS AND RS), MODEL ML600/S: SINGLE LIGHT HEAD, ML600/SS: SINGLE LIGHT HEAD, ML600/1D): DOUB
STELLAR
VISIONARY 2000
CASTLE SURGICAL LIGHT, MODEL 3000
MILLENNIUM GOLD
CHROMOPHARE D 530 LDR SURGICAL LIGHT
CHROMOPHARE D500, D530, D650
DRAGER SOLA SERIES, MODELS 1000/700/500/300
ALM PRISMALIX (PRX) SURGICAL LIGHT
BRIGHTSTAR
GETINGE/CASTLE OPTIVIEW SERIES SURGICAL LIGHT
CHROMOPHARE D 500, CHROMOPHARE D 530
HANAULUX BLUE 75 AND HANAULUX BLUE 120

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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