Stl International, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3022192
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3022192
- Address
- 22503 97th St E, Bonney Lake, WA, 98391
Frequently asked questions
How many devices does STL INTERNATIONAL, INC. have in the registry?
The registry currently lists 1 device for STL INTERNATIONAL, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list STL INTERNATIONAL, INC.'s devices?
Among its 1 most recently registered device, STL INTERNATIONAL, INC. has devices listed in FDA 510(k) (1 device).
What risk classes do STL INTERNATIONAL, INC.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for STL INTERNATIONAL, INC.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from STL INTERNATIONAL, INC. in the registry?
The most recently registered devices listed for STL INTERNATIONAL, INC. include Teeter Manual Inversion Table; Teeter Gravity Boots; Teeter Forward Rotation Decompression Device; Teeter Portable Decompression Device; Teeter Horizontal Decompression Table.