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American Surgical Laser, Inc.

United StatesFDA applicant, unverified

Devices
5

What American Surgical Laser, Inc. makes

American Surgical Laser, Inc. manufactures CO₂ microsurgical lasers designed for precision dermatological procedures, general surgery, podiatry, gynecological applications, and otolaryngology. These devices are intended for controlled tissue ablation, coagulation, and vaporisation in clinical settings.

The company’s portfolio includes Class I and Class II devices, all of which are listed via the FDA’s 510(k) pathway. These lasers are regulated under US medical device standards and are intended for use within the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does American Surgical Laser, Inc. have in the registry?

The registry currently lists 5 devices for American Surgical Laser, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list American Surgical Laser, Inc.'s devices?

Among its 5 most recently registered devices, American Surgical Laser, Inc. has devices listed in FDA 510(k) (5 devices).

What risk classes do American Surgical Laser, Inc.'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for American Surgical Laser, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from American Surgical Laser, Inc. in the registry?

The most recently registered devices listed for American Surgical Laser, Inc. include MINUTEMAN CO2 MICROSURG LASER DERMATOL-, MINUTEMAN CO2 MICROSURG LASER GEN SURG, MINUTEMAN C02 MICROSURG LASER PODIATRY and MINUTEMAN CO2 MICROSURGICAL LASER GYN.

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