Aperta, LLC
Country not established
- Devices
- 1
What Aperta, LLC makes
Aperta, LLC manufactures the Wittmann PATCH, a medical device designed for transdermal drug delivery or monitoring applications, utilizing adhesive patch technology for skin contact.
The Wittmann PATCH is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Wittmann Patch Ref K093166
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aperta, LLC have in the registry?
The registry currently lists 1 device for Aperta, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aperta, LLC's devices?
Among its 1 most recently registered device, Aperta, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Aperta, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Aperta, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aperta, LLC in the registry?
The most recently registered devices listed for Aperta, LLC include WITTMANN PATCH.