Universal Technology Systems, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Universal Technology Systems, Inc. makes
Universal Technology Systems, Inc. manufactures electrical muscle stimulation devices, including the PGS 1500, PGS-4000, and PGS 2000 TENS units. These products are designed for transcutaneous electrical nerve stimulation (TENS) and muscle stimulation therapy, intended to manage pain and promote muscle activation.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
- 510(k) 510(k)
Electrical Muscle Stimulator Device ( Pgs-4000) Ref K980346
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Universal Technology Systems, Inc. have in the registry?
The registry currently lists 3 devices for Universal Technology Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Universal Technology Systems, Inc.'s devices?
Among its 3 most recently registered devices, Universal Technology Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Universal Technology Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Universal Technology Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Universal Technology Systems, Inc. in the registry?
The most recently registered devices listed for Universal Technology Systems, Inc. include UTS ELECTRICAL MUSCLE STIMULATION DEVICE-PGS 1500, ELECTRICAL MUSCLE STIMULATOR DEVICE ( PGS-4000) and ELECTRICAL MUSCLE STIMULATOR--PGS 2000 TENS DEVICE.