The Spritz Co.
Country not established
- Devices
- 1
What The Spritz Co. makes
The Spritz Co. manufactures The Spritz Bath, a Class I medical device designed for therapeutic bathing applications, including wound care and skin decontamination in clinical settings.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class I device and is listed in the US regulatory database. The Spritz Co. is headquartered in the United States.
Catalogue
The Spritz Bath Ref K912179
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Spritz Co. have in the registry?
The registry currently lists 1 device for The Spritz Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Spritz Co.'s devices?
Among its 1 most recently registered device, The Spritz Co. has devices listed in FDA 510(k) (1 device).
What risk classes do The Spritz Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Spritz Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from The Spritz Co. in the registry?
The most recently registered devices listed for The Spritz Co. include THE SPRITZ BATH.