Nanoplas, Inc.
Country not established
- Devices
- 1
What Nanoplas, Inc. makes
Nanoplas, Inc. manufactures a saline wound wash, a sterile solution designed for cleaning and irrigating wounds to remove debris and contaminants during medical procedures.
The saline wound wash is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Saline Wound Wash Ref K112666
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nanoplas, Inc. have in the registry?
The registry currently lists 1 device for Nanoplas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nanoplas, Inc.'s devices?
Among its 1 most recently registered device, Nanoplas, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Nanoplas, Inc. in the registry?
The most recently registered devices listed for Nanoplas, Inc. include SALINE WOUND WASH.