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Dyansys, Inc.

Also registered as Dyansys Corp

United StatesFDA 510(k) applicant, unverified

Devices
15

What Dyansys, Inc. makes

Dyansys, Inc. manufactures electrostimulation devices for pain management and nerve stimulation, including portable and fixed systems like the ECSCOPE 200 and PORTABLE ECSCOPE 12I. Their portfolio includes transcutaneous electrical nerve stimulation (TENS) units such as ANSiStim-PP and ANSISTIM, as well as drug delivery devices like Drug Relief and First Relief for localized pain relief. These products are designed for at-home or clinical use to alleviate chronic or acute pain through electrical stimulation or topical medication application.

The company’s devices are classified under FDA Class II and Class U (unclassified) categories, with regulatory submissions supported by 510(k) clearances. Their products are listed in the FDA’s 510(k) registry, indicating compliance with U.S. medical device regulations. Dyansys, Inc. is headquartered in the United States.

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

Catalogue15

Newest first, rows 1-15 of 15

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  • Ecscope 200 Ref K091397

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

  • Primary Relief Ref K221425

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

  • ANSiStim-PP Ref K170391

    Unclassified
    Active 510(k) 510(k) —

  • Portable Ecscope 12I Ref K080036

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

  • Drug Relief v1 Ref K221231

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

  • Primary Relief Ref K213188

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

  • Drug Relief v1 Ref K211971

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

  • Drug Relief Ref K173861

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

  • First Relief Ref K212859

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

  • Ansistim Ref K141168

    Unclassified
    Active 510(k) 510(k) —

  • ANSiStim-PP Ref K220397

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

  • First Relief v1 Ref K202940

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

  • Portable Ecscope Ref K072353

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

  • The Portable Ansiscope Ref K071168

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

  • Ecscope 100 Ref K091358

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

Rows 1-15 of 15

Frequently asked questions

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

The registry currently lists 15 devices for Dyansys, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dyansys, Inc.'s devices?

Among its 15 most recently registered devices, Dyansys, Inc. has devices listed in FDA 510(k) (15 devices).

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

Among its 15 most recently registered devices, the classes recorded for Dyansys, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Dyansys, Inc. include ECSCOPE 200, Primary Relief, ANSiStim-PP and PORTABLE ECSCOPE 12I.

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