Endosurgical Development Corp.
Country not established
- Devices
- 1
What Endosurgical Development Corp. makes
Endosurgical Development Corp. manufactures the COOL LIGHT 300, a surgical light designed for endoscopic procedures to provide illumination within confined spaces during minimally invasive surgeries.
The COOL LIGHT 300 is classified as a Class II medical device and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
Cool Light 300 Ref K935423
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endosurgical Development Corp. have in the registry?
The registry currently lists 1 device for Endosurgical Development Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endosurgical Development Corp.'s devices?
Among its 1 most recently registered device, Endosurgical Development Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Endosurgical Development Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Endosurgical Development Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endosurgical Development Corp. in the registry?
The most recently registered devices listed for Endosurgical Development Corp. include COOL LIGHT 300.