Shenzhen Bestman Instrument Co., Ltd. is one of 2048 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Shenzhen Bestman Instrument Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Doppler FHR Detector (BF-500D+, BF-560), DOPPLER FETAL HEARTBEAT RATE DETECTOR
2
Total
2
Cleared
0
Denied
Shenzhen Bestman Instrument Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Guangdong, CN.
Latest FDA clearance: Jun 2025. Active since 2010. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Shenzhen Bestman Instrument Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Shenzhen Bestman Instrument Co., Ltd.
2 devices