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: LYL FDA class 2

Accessories, Solution, Ultrasonic Cleaners For Lenses

Ophthalmic

View full classification →

Ultrasonic Lens Cleaner Solution Accessories (product code LYL) are ophthalmic products including cleaning solutions and accessories used in conjunction with ultrasonic cleaning devices for contact lenses, facilitating the removal of deposits and maintaining lens hygiene. Regulated under 21 CFR 886.5928 and classified as a Class 2 device, they require a 510(k) premarket notification and are eligible for third-party review. The devices fall under the Ophthalmic specialty. They are not implants and are not life-sustaining.

510(k) Clearances

22 matches
K Number
Device Name
3N Contact Lenses Adjunct Cleaner
VueSonic One Contact Lens Cleaning System, VueSonic Advance 2 Contact Lens Cleaning System
BPZ02 MULTIPURPOSE SOLUTION
AUTOLENS CLEANING AND DISINFECTING UNIT
AOSEPT CLEAR CARE CLEANING AND DISINFECTING SOLUTION
RENUT MULTIPLUS MULLTI-PURPOSE SOLUTION
CONTACLAIR MULTI-PURPOSE CONTACT LENS SOLUTION
PURILENS SYSTEM FOR CLEANING AND DISINFECTING CONTACT LENSES
LENSERVER AUTOMATIC CONTACT LENS CLEANING ACCESSORY
SOFTMATE AUTOMATIC LENS CLEANING UNIT, CLENSATRON 700 CL AUTOMATIC CONTACT LENS CLEANER, VISONIC DOME, LENSONIC CONTACT
ACU-CLENS CLEANING SYSTEM FOR CONTACT LENS CLEANING
NEW COMFORT CONTACT LENS CARE ACCESSORY
OPTI PADS
CONTACT LENS CLEANING ACCESSORY
LENSONIC(TM) CONTACT LENS CARE ACCESSORY
THE CLEANER ACCESSORY
TURBOTRON 20/20
EASY EYES TM CONTACT LENS CLEANING MACHINE
THE VISONIC DOME(TM)
SPIN-CLEAN CLEANING UNIT
CLENSATRON AUTOMATIC CONTACT LENS CLEANER
LENZ CLENZER

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.

Popular Product Codes

Commonly searched