The Soule Co
Also registered as The Soule Co., Inc.
Country not established FDA establishment FEI 1000525333
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Rapid-Foam Ref K952457
510(k) 510(k)
Company details
- FDA FEI number
- 1000525333
- Address
- 26543 Wild Fern Cir., LUTZ, FL, 33559
Frequently asked questions
How many devices does THE SOULE CO have in the registry?
The registry currently lists 1 device for THE SOULE CO. Devices recorded under merged duplicate company entries are counted once.
Which registries list THE SOULE CO's devices?
Among its 1 most recently registered device, THE SOULE CO has devices listed in FDA 510(k) (1 device).
What risk classes do THE SOULE CO's devices fall under?
Among its 1 most recently registered device, the classes recorded for THE SOULE CO's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from THE SOULE CO in the registry?
The most recently registered devices listed for THE SOULE CO include RAPID-FOAM.