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Light Age, Inc.

United StatesFDA applicant, unverified

Devices
7

What Light Age, Inc. makes

Light Age, Inc. manufactures laser systems and devices for dermatological and aesthetic treatments, including the EPICARE-DUO Laser System, Q-CLEAR Laser (Model 701-1101), and various EPICARE Alexandrite Laser models (501-1H, 501-SP, 501-LP, 501-LPX). Their portfolio also includes the EPICARE YAG, ALEX TA2 Eraser, and standalone Q-CLEAR device, designed for procedures such as hair removal, pigmentation treatment, and skin resurfacing.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States, with its products authorised for commercial distribution in the US market.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Light Age, Inc. have in the registry?

The registry currently lists 7 devices for Light Age, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Light Age, Inc.'s devices?

Among its 7 most recently registered devices, Light Age, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Light Age, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Light Age, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Light Age, Inc. in the registry?

The most recently registered devices listed for Light Age, Inc. include EPICARE-DUO LASER SYSTEM, LIGHT AGE Q-CLEAR LASER, MODEL 701-1101, LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX and EPICARE YAG.

Generated automatically from registry data and not verified by a human reviewer.