Guangzhou Hehong Biotech Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Guangzhou Hehong Biotech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Minvitro Embryo Transfer Catheters (ETCA23175, ETCA23175-C, ETCB20175, ETCB20175-C, ETCB20175-ET, ETCB20175-ET-C), Minvitro® Vitrification Straw (MVT-VSN series, including MVT-VSNR, MVT-VSNY, MVT-VSNB, MVT-VSNG, MVT-VSNP)
2
Total
2
Cleared
0
Denied
Guangzhou Hehong Biotech Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Guangzhou, CN.
Latest FDA clearance: Feb 2026. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Guangzhou Hehong Biotech Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Manton Business and Technology Services as regulatory consultant.
FDA 510(k) Regulatory Record - Guangzhou Hehong Biotech Co., Ltd.
2 devices