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Paranamics, Inc.

United StatesFDA applicant, unverified

Devices
2

What Paranamics, Inc. makes

Paranamics, Inc. manufactures muscle stimulators, including the HAELAN 340 and EMS 300 models, designed for therapeutic electrical stimulation of muscle tissue.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Haelan 340 Muscle Stimulator Ref K902371

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ems 300 Muscle Stimulators Ref K890434

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

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

The registry currently lists 2 devices for Paranamics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Paranamics, Inc.'s devices?

Among its 2 most recently registered devices, Paranamics, Inc. has devices listed in FDA 510(k) (2 devices).

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

Among its 2 most recently registered devices, the classes recorded for Paranamics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Paranamics, Inc. include HAELAN 340 MUSCLE STIMULATOR and EMS 300 MUSCLE STIMULATORS.

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