Shenzhen Bestman Instrument Co., Ltd.

FDA Regulatory Profile

Shenzhen Bestman Instrument Co., Ltd. appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 26, 2025.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K242846Doppler FHR Detector (BF-500D+, BF-560)June 26, 2025
K090510DOPPLER FETAL HEARTBEAT RATE DETECTORApril 29, 2010