Phoenix Instruments Div.
Country not established
- Devices
- 1
What Phoenix Instruments Div. makes
Phoenix Instruments Div. manufactures manual surgical instruments designed for use in clinical procedures. These tools are intended for general surgical applications, including cutting, grasping, and manipulating tissue during operations.
The company’s portfolio is regulated under FDA Class I devices, with products listed via the 510(k) pathway. These instruments are included in the FDA’s regulatory registry. The manufacturer is based in the United States.
Catalogue
Manual Surgical Instruments Ref K920263
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Phoenix Instruments Div. have in the registry?
The registry currently lists 1 device for Phoenix Instruments Div.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Phoenix Instruments Div.'s devices?
Among its 1 most recently registered device, Phoenix Instruments Div. has devices listed in FDA 510(k) (1 device).
What risk classes do Phoenix Instruments Div.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Phoenix Instruments Div.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Phoenix Instruments Div. in the registry?
The most recently registered devices listed for Phoenix Instruments Div. include MANUAL SURGICAL INSTRUMENTS.