Diversified Healthcare Development LLC.
United Statesfrom the FDA registration address FDA establishment FEI 3001541016
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Diversified Healthcare Development LLC. makes
Diversified Healthcare Development LLC manufactures systems designed to assess balance and cognitive function, including the Koresway and Korebalance Premiere. These devices are intended for clinical or research use to evaluate patient performance in stability and cognitive tasks.
The company’s portfolio includes devices classified as Class I and Unclassified (U) under FDA regulations, all of which are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Company details
- FDA FEI number
- 3001541016
- Address
- 60 Corporate Ln, Independence, VA, 24348
Frequently asked questions
How many devices does Diversified Healthcare Development LLC. have in the registry?
The registry currently lists 3 devices for Diversified Healthcare Development LLC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Diversified Healthcare Development LLC.'s devices?
Among its 3 most recently registered devices, Diversified Healthcare Development LLC. has devices listed in FDA GUDID (3 devices).
What risk classes do Diversified Healthcare Development LLC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Diversified Healthcare Development LLC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Diversified Healthcare Development LLC. in the registry?
The most recently registered devices listed for Diversified Healthcare Development LLC. include Korebalance Mobile KB05B, Koresway KB05 and Korebalance Premiere KB01.