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Physio Technology, Inc.

United StatesFDA applicant, unverified

Devices
10

What Physio Technology, Inc. makes

Physio Technology, Inc. manufactures electrotherapy devices, including vacuum electrode systems, interferential therapy units, muscle stimulators, and sound therapy apparatus. Their portfolio includes units for electrical muscle stimulation (e.g., OMNISTIM III, AUTOMOVE/OMNISTIM IV), biofeedback devices (e.g., MYOMETER EMG), and combined therapy systems (e.g., OMNISTIM II). Additional offerings cover pulsed therapy units (e.g., MEGA PULSE) and sound-based therapy (e.g., OMNISOUND 3000).

The company’s devices are classified under FDA’s Class I and Class II categories, with most requiring 510(k) clearance. Their products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

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

The registry currently lists 10 devices for Physio Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Physio Technology, Inc.'s devices?

Among its 10 most recently registered devices, Physio Technology, Inc. has devices listed in FDA 510(k) (10 devices).

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

Among its 10 most recently registered devices, the classes recorded for Physio Technology, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Physio Technology, Inc. include OMNIVAC (VACUUM ELECTRODE SYSTEM), OMNISTIM III INTERFERENTIAL THERAPY, MEGA PULSE THERAPY UNIT and MODIFIED OMNISTIM(TM) ELECTRICAL MUSCLE STIMULATOR.

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