Theodore Barash
Country not established
- Devices
- 1
What Theodore Barash makes
Theodore Barash manufactures compression and support garments with embedded magnets, designed for the lower back, knee, and ankle. These products are intended to provide targeted support and relief for musculoskeletal discomfort.
The company’s portfolio is regulated under FDA Class I devices and requires 510(k) clearance. The products are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Theodore Barash have in the registry?
The registry currently lists 1 device for Theodore Barash. Devices recorded under merged duplicate company entries are counted once.
Which registries list Theodore Barash's devices?
Among its 1 most recently registered device, Theodore Barash has devices listed in FDA 510(k) (1 device).
What risk classes do Theodore Barash's devices fall under?
Among its 1 most recently registered device, the classes recorded for Theodore Barash's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Theodore Barash in the registry?
The most recently registered devices listed for Theodore Barash include BACK IN ACTION COMPRESSION & SUPPORT WITH MAGNETS FOR THE LOWER BACK, KNEE AND ANKLE.