Universal Gym Equipment, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Universal Gym Equipment, Inc. makes
Universal Gym Equipment, Inc. manufactures the Ankle Reflex Treatment Unit (ARTU) and musculoskeletal evaluation and rehabilitation devices designed for physical therapy and conditioning. These products are intended for assessing and treating musculoskeletal conditions through targeted exercises and reflex stimulation.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions supported by 510(k) clearances. These products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Ankle Reflex Treatment Unit (Artu) Ref K873658
510(k) 510(k)- 510(k) 510(k)
Frequently asked questions
How many devices does Universal Gym Equipment, Inc. have in the registry?
The registry currently lists 2 devices for Universal Gym Equipment, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Universal Gym Equipment, Inc.'s devices?
Among its 2 most recently registered devices, Universal Gym Equipment, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Universal Gym Equipment, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Universal Gym Equipment, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Universal Gym Equipment, Inc. in the registry?
The most recently registered devices listed for Universal Gym Equipment, Inc. include ANKLE REFLEX TREATMENT UNIT (ARTU) and MUSCULOSKELETAL EVALUATION REHABILITATION/CONDITIO.