River'S Edge Pharmaceuticals, LLC
Country not established
- Devices
- 1
What River'S Edge Pharmaceuticals, LLC makes
River’s Edge Pharmaceuticals, LLC produces modifications to the Zenieva device, a Class I medical product designed for pharmaceutical or compounding applications.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices listed in the U.S. regulatory system. The company is based in the United States.
Catalogue
Modification To Zenieva Ref K083721
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does River'S Edge Pharmaceuticals, LLC have in the registry?
The registry currently lists 1 device for River'S Edge Pharmaceuticals, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list River'S Edge Pharmaceuticals, LLC's devices?
Among its 1 most recently registered device, River'S Edge Pharmaceuticals, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do River'S Edge Pharmaceuticals, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for River'S Edge Pharmaceuticals, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from River'S Edge Pharmaceuticals, LLC in the registry?
The most recently registered devices listed for River'S Edge Pharmaceuticals, LLC include MODIFICATION TO ZENIEVA.