Rythmic and Rythmic UV

by Essilor Intl. 510(k)

Active United States

510(k) K003170

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Traditional	NumberK003170	Date15 Dec 2000Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number: K003170
FDA Product Code: LPL

Device Class: Class II
Regulation: 21 CFR Part 886.5925
Advisory Committee: Ophthalmic
FDA Decision: SESE Substantially Equivalent

Other devices from Essilor Intl.

Varilux Visionprint System (Vps)

Class II