S&G Biotech, Inc. - FDA 510(k) Cleared Devices
2
Total
0
Cleared
0
Denied
S&G Biotech, Inc. has 0 FDA 510(k) cleared medical devices. Based in Yongin-Si, KR.
Latest FDA clearance: Jun 2025. Active since 2023. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by S&G Biotech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtech Group, LLC as regulatory consultant.
2 devices