Medical Device Manufacturer · US , Oakland , CA

Xintec Corporation - FDA 510(k) Cleared Devices

26 submissions · 26 cleared · Since 1990

Recent clearances: VECTRA PLUS LASER SYSTEM AND ACCESSORIES, POLARIS DIODE LASER SYSTEM AND ACCESSORIES, PROTEGE II ER: YAG LASER SYSTEM AND ACCESSOIES (UPGRADE)

26
Total
26
Cleared
0
Denied

FDA 510(k) Regulatory Record - Xintec Corporation General & Plastic Surgery ✕

26 devices
1-12 of 26
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