Vigeon Technology Co., Ltd. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Vigeon Technology Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Vigeon Laparoscopic Universal Smoke Evacuator (VG003)
1
Total
1
Cleared
0
Denied
Vigeon Technology Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Taipei City, TW.
Latest FDA clearance: May 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vigeon Technology Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by ZhengCheng Consulting Limited Company as regulatory consultant.
FDA 510(k) Regulatory Record - Vigeon Technology Co., Ltd.
1 devices