Alton Dean Medical, Inc.
Country not established
- Devices
- 1
What Alton Dean Medical, Inc. makes
Alton Dean Medical, Inc. manufactures the ORCEPAD, a medical device designed for use in surgical procedures, specifically for electrocautery applications to control bleeding and tissue dissection.
The ORCEPAD is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Orcepad Ref K875123
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alton Dean Medical, Inc. have in the registry?
The registry currently lists 1 device for Alton Dean Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alton Dean Medical, Inc.'s devices?
Among its 1 most recently registered device, Alton Dean Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Alton Dean Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Alton Dean Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alton Dean Medical, Inc. in the registry?
The most recently registered devices listed for Alton Dean Medical, Inc. include ORCEPAD.