Curwood, Inc.
Country not established
- Devices
- 1
What Curwood, Inc. makes
Curwood, Inc. manufactures the MEDI-OXIDE Sterilization Pouch from its MEDI-PLUS line, a sterile barrier pouch designed for medical device sterilization processes.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance in the United States.
Catalogue
Medi-Oxide Sterilzation Pouch From Medi-Plus Ref K953749
510(k) 510(k)
Frequently asked questions
How many devices does Curwood, Inc. have in the registry?
The registry currently lists 1 device for Curwood, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Curwood, Inc.'s devices?
Among its 1 most recently registered device, Curwood, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Curwood, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Curwood, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Curwood, Inc. in the registry?
The most recently registered devices listed for Curwood, Inc. include MEDI-OXIDE STERILZATION POUCH FROM MEDI-PLUS.