Vigeon Technology Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Vigeon Technology Co., Ltd. makes
Vigeon Technology Co., Ltd. manufactures the Vigeon Laparoscopic Universal Smoke Evacuator (VG003), a device designed for smoke evacuation during laparoscopic surgical procedures to improve visibility and reduce exposure to surgical smoke for patients and staff.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vigeon Technology Co., Ltd. have in the registry?
The registry currently lists 1 device for Vigeon Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vigeon Technology Co., Ltd.'s devices?
Among its 1 most recently registered device, Vigeon Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Vigeon Technology Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Vigeon Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vigeon Technology Co., Ltd. in the registry?
The most recently registered devices listed for Vigeon Technology Co., Ltd. include Vigeon Laparoscopic Universal Smoke Evacuator (VG003).