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Btl

Country not established

Devices
4

What Btl makes

The company manufactures Class II laser-based medical devices, including systems for aesthetic treatments such as skin resurfacing, hair removal, and tattoo removal, as well as medical-grade laser and radiofrequency devices for dermatological procedures.

These devices are regulated under the FDA’s 510(k) pathway as Class II medical devices and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

  • Btl-785F Ref K193201

    Class II
    Active 510(k) 510(k) II
  • Btl-703-2 Ref K200382

    Class II
    Active 510(k) 510(k) II
  • Btl-899ST Ref K202199

    Class II
    Active 510(k) 510(k) II
  • Btl-899 Ref K192224

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Btl have in the registry?

The registry currently lists 4 devices for Btl. Devices recorded under merged duplicate company entries are counted once.

Which registries list Btl's devices?

Among its 4 most recently registered devices, Btl has devices listed in FDA 510(k) (4 devices).

What risk classes do Btl's devices fall under?

Among its 4 most recently registered devices, the classes recorded for Btl's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Btl in the registry?

The most recently registered devices listed for Btl include BTL-785F, BTL-703-2, BTL-899ST and BTL-899.

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