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Vts, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
5

What Vts, Inc. makes

Vts, Inc. manufactures vacuum therapy systems and vacuum erection devices, including the SE-200, SE-300 Vacuum Therapy System, VT-1, and SE-100 Vacuum Erection Device.

The company's devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

  • V.T.S., Inc. (V.T.-3) Ref K992442

    Class II
    Active 510(k) 510(k) II
  • Se-200 Ref K012620

    Class II
    Active 510(k) 510(k) II
  • Se-300 Vacuum Therapy System Ref K012639

    Class II
    Active 510(k) 510(k) II
  • Vt-1 Ref K012619

    Class II
    Active 510(k) 510(k) II
  • Se-100 Vacuum Erection Device Ref K012662

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

Frequently asked questions

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

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

Which registries list Vts, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Vts, Inc. include V.T.S., INC. (V.T.-3), SE-200, SE-300 VACUUM THERAPY SYSTEM and VT-1.

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