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M. D. Supply, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
3

What M. D. Supply, Inc. makes

M. D. Supply, Inc. manufactures the Comfortron, a transcutaneous electrical nerve stimulation (TENS) device, and its variant, the Comfortron PT (TENS). These devices are designed for pain management through electrical stimulation.

The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Comfortron Ref K925821

    Class II
    Active 510(k) 510(k) II
  • Comfortron Ref K862092

    Class II
    Active 510(k) 510(k) II
  • Comfortron Pt (Tens) Ref K911066

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

Frequently asked questions

How many devices does M. D. Supply, Inc. have in the registry?

The registry currently lists 3 devices for M. D. Supply, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list M. D. Supply, Inc.'s devices?

Among its 3 most recently registered devices, M. D. Supply, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do M. D. Supply, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for M. D. Supply, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from M. D. Supply, Inc. in the registry?

The most recently registered devices listed for M. D. Supply, Inc. include COMFORTRON and COMFORTRON PT (TENS).

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