Koike Medical Co.
Country not established
- Devices
- 1
What Koike Medical Co. makes
Koike Medical Co. manufactures the SANPO I, a medical device designed for specific orthopedic or spinal applications, likely used in surgical procedures to support bone stabilization or fixation.
The SANPO I is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Sanpo I Ref K964541
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Koike Medical Co. have in the registry?
The registry currently lists 1 device for Koike Medical Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Koike Medical Co.'s devices?
Among its 1 most recently registered device, Koike Medical Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Koike Medical Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Koike Medical Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Koike Medical Co. in the registry?
The most recently registered devices listed for Koike Medical Co. include SANPO I.