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Guangzhou Red Pine Medical Instrument Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251951Single-Use Video Flexible Ureterorenoscope (RP-U-C03R9, RP-U-C03R3, RP-U-C03S9, RP-U-C03S3); EndoscoDecember 16, 2025
K252176Single-Use Video Flexible Cysto-Nephroscope (RP-U-C01F, RP-U-C01FS)August 8, 2025
K243321Endoscopic Video Image Processor (RP-IPD-V1000F)February 7, 2025
K241987Single-Use Video Hysteroscope (RP-G-C24, RP-G-C0101)August 2, 2024
K241500Endoscopic Video Image Processor (RP-IPD-V2000EF); Single-Use Video Flexible Cysto-Nephroscope (RP-UJuly 12, 2024
K240663Single-Use Video Flexible Cystoscope (RP-U-C0201/RP-U-C0201S)June 21, 2024
K232043Endoscopic Video Image Processor (RP-IPD-V2000A, RP-IPD-V2000B, RP-IPD-V2000C, RP-IPD-V2000D), SingFebruary 16, 2024
K232003Endoscopic Video Image Processor, Single-Use Video HysteroscopeFebruary 12, 2024
K221158Single-Use Video Flexible Ureterorenoscope SystemMarch 6, 2023