Neogen Technologies, Inc.
Country not established
- Devices
- 1
What Neogen Technologies, Inc. makes
Neogen Technologies, Inc. manufactures the NEOGEN ONE, a closed wound drain system designed for postoperative fluid management in surgical procedures.
The company’s products are regulated as Class II medical devices in the U.S. and are listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neogen Technologies, Inc. have in the registry?
The registry currently lists 1 device for Neogen Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neogen Technologies, Inc.'s devices?
Among its 1 most recently registered device, Neogen Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neogen Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neogen Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neogen Technologies, Inc. in the registry?
The most recently registered devices listed for Neogen Technologies, Inc. include NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900.