Whele LLC
United Statesfrom the FDA registration address FDA establishment FEI 3016774562
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Whele LLC makes
Whele LLC manufactures ankle/foot orthoses, including the AZMED device, designed to support and correct foot and ankle alignment for patients.
The company’s products are classified as Class I medical devices and are listed in the FDA’s Unique Device Identifier (UDI) database, adhering to U.S. regulatory requirements.
Catalogue
- Registry: GUDID
Company details
- FDA FEI number
- 3016774562
- Address
- 801 Barton Springs Rd, Austin, TX, 78704
Frequently asked questions
How many devices does Whele LLC have in the registry?
The registry currently lists 1 device for Whele LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Whele LLC's devices?
Among its 1 most recently registered device, Whele LLC has devices listed in FDA GUDID (1 device).
What risk classes do Whele LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Whele LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Whele LLC in the registry?
The most recently registered devices listed for Whele LLC include AZMED PXAZ-000004.