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: FSS FDA class 2

Light, Surgical, Floor Standing

General, Plastic Surgery

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A floor-standing surgical light is a mobile or fixed-position high-intensity lighting unit used to illuminate the surgical field in operating rooms and procedure areas. 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 FSS, regulated under 21 CFR 878.4580, within the General, Plastic Surgery medical specialty. No special flags apply to this device.

510(k) Clearances

20 matches
K Number
Device Name
ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)
NEXT GENERAL M20 SURGICAL LIGHT; NEXT GENERATION M16 MINOR SURGERY LIGHT; NEXT GENERATION SPOTLIGHT; NEXT GENERATION M8
AESCULAP XENON LIGHT SOURCE
CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCE
VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR
CERMAX300 LIGHTSOURCE
XENON 300MX
HANAULUX BLUE 80 HOSPITAL
Q-5000
LIGHTSOURCE OR ILLUMINATOR
TRI*STAR
AC POWERED AND BATTERY POWERED MEDICAL EXAM. LIGHT
MODEL FEL5100 FLOOR LIGHT
FLOOR STANDING, OPERATING AND EXAMINING LIGHT
KINETIC MODEL 330
KINETIC MODEL 132
FLOOR LIGHT
LIGHT, SURGICAL, FLOOR STANDING
GEMINI SURGICAL LIGHT
MINOR SURGERY LIGHT MODEL 2112

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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