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Actegy, Ltd.

Country not established FDA

Actegy, Ltd. is a medical device manufacturer, with 19 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.

Devices
19
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 12
  • FDA 510(k) 7

A device listed in two registries counts in both.

Device classes
  • FDA Class II 19

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Actegy, Ltd. makes

Actegy, Ltd. manufactures line-powered transcutaneous electrical stimulation (TENS) systems for pain management and neuromuscular stimulation, including dedicated analgesic TENS devices. Their portfolio also includes single-use TENS electrodes and respiratory muscle training masks for targeted therapy. Additional products focus on circulation support and joint-specific therapy, such as knee pads for arthritis relief.

The company’s devices are classified as Class II under FDA regulations and are authorised via 510(k) clearances and the FDA’s Unique Device Identifier (UDI) system. These products are listed in the U.S. regulatory database and comply with applicable U.S. medical device standards.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue19

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FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Actegy Limited Bracknell · GB FEI 3010078417

Frequently asked questions

How many devices does Actegy, Ltd. have in the registry?

The registry currently lists 19 devices for Actegy, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Actegy, Ltd.'s devices?

Among its 19 most recently registered devices, Actegy, Ltd. has devices listed in FDA 510(k) (7 devices) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Actegy, Ltd.'s devices fall under?

Among its 19 most recently registered devices, the classes recorded for Actegy, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Actegy, Ltd. in the registry?

The most recently registered devices listed for Actegy, Ltd. include Revitive Electrode Body Pads 2044, Revitive Circulation Booster RIX, Aerosure 3481AJ and Revitive Advanced RMV.

Which FDA establishments are linked to Actegy, Ltd.?

1 FDA establishment is linked to Actegy, Ltd. in the registry; they are listed on the company page.

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