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: OOE FDA class 2

Ophthalmic Femtosecond Laser

Ophthalmic

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The Ophthalmic Femtosecond Laser (product code OOE) is a Class 2 ophthalmic device regulated under 21 CFR 886.4390 in the Ophthalmic specialty (OP), cleared via 510(k). It is used for precise cutting or ablation of ocular tissue, specifically indicated for anterior capsulotomy during cataract surgery, enabling highly accurate circular incisions in the lens capsule. The device is not an implant and is not life-sustaining.

510(k) Clearances

46 matches
K Number
Device Name
LenSx Laser System (8065998162)
ELITA™ Femtosecond Laser System, ELITA™ Patient Interface
Catalys™ Precision Laser System
ALLY Adaptive Cataract Treatment System
CATALYS Precision Laser system
FEMTO LDV Z8 Femtosecond Surgical Laser
CATALYS Precision Laser System
VICTUS Femtosecond Laser Platform
Catalys Precision Laser System
LENSAR Laser System - fs 3D (LLS-fs 3D)
Catalys Precision Laser System
LENSAR Laser System - fs 3D (LLS-fs 3D)
LenSx Laser System
LENSAR Laser System - fs 3D (LLS-fs 3D)
VICTUS Femtosecond Laser Platform
Catalys Precision Laser System
LENSAR Laser System – fs 3D (LLS-fs 3D)
Catalys Precision Laser System
LENSAR Laser System - fs 3D (LLS-fs 3D)
LenSx Laser System
LenSX Laser System
Catalys Precision Laser System
FEMTO LDV Z8 Surgical Laser
LENSAR Laser System - fs 3D (LLS-fs 3D)
VICTUS Femtosecond Laser Platform
LENSAR Laser System - fs 3D
VICTUS FEMTOSECOND LASER PLATFORM
WAVELIGHT FS200 LASER SYSTEM
OPTIMEDICA CATALYS PRECISION LASER SYSTEM
VICTUS FEMTOSECOND LASER PLATFORM
VICTUS FEMTOSECOND LASER PLATFORM
TBD
VICTUS FEMTOSECOND LASER PLATFORM
LENSX LASER SYSTEM
CATALYS PRECISION LASER SYSTEM
VICTUS LASER PLATFORM
TBD
OPTIMEDICA CATALYS PRECISION LASER SYSTEM
FEMTEC LASER SYSTEM FOR CAPSULOTOMY
TBD
LENSAR LASER SYSTEM FOR ANTERIOR CAPSULOTOMY
LENSX LASER SYSTEM
LENSAR LASER SYSTEM
LENSX 550 LASER SYSTEM. MODEL 550
LENSX 550 LASER SYSTEM
LENSX 550 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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