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Shaser, Inc.

United StatesFDA applicant, unverified

Devices
10

What Shaser, Inc. makes

Shaser, Inc. manufactures medical-grade hair removal systems, including the SHASER HRS2 RX, LUMENA FH, and variants of the SHASER V-MINI series, designed for professional use in clinical and aesthetic settings. Their product line also includes intense pulsed light (IPL) systems, such as the Shaser Skin Beauty IPL Family and SkinREJUV, intended for acne treatment and skin rejuvenation procedures.

These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company’s portfolio is listed in the FDA’s 510(k) registry, and Shaser, Inc. is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

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

The registry currently lists 10 devices for Shaser, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shaser, Inc.'s devices?

Among its 10 most recently registered devices, Shaser, Inc. has devices listed in FDA 510(k) (10 devices).

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

Among its 10 most recently registered devices, the classes recorded for Shaser, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Shaser, Inc. include SHASER HRS2 RX HAIR REMOVAL SYSTEM, Shaser Skin Beauty Intense Pulsed Light System Family for Acne, SHASER V-MINI RX and LUMENA FH HAIR REMOVAL SYSTEM.

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