Surgimage Corporation
TaiwanFDA applicant, unverified
- Devices
- 1
What Surgimage Corporation makes
Surgimage Corporation manufactures the SIM 1000H Fluorescence Imaging Platform, a device designed for intraoperative imaging to enhance visualization of tissues during surgical procedures.
The SIM 1000H is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in Taiwan.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Surgimage Corporation have in the registry?
The registry currently lists 1 device for Surgimage Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgimage Corporation's devices?
Among its 1 most recently registered device, Surgimage Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Surgimage Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Surgimage Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgimage Corporation in the registry?
The most recently registered devices listed for Surgimage Corporation include SURGIMAGE SIM 1000H Fluorescence Imaging Platform.