Alton (Shanghai) Medical Instruments Co., Ltd.

FDA Regulatory Profile

Alton (Shanghai) Medical Instruments Co., Ltd. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 18, 2025.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K243039Ureteral Stents (AF-D series)June 18, 2025
K242635Endoscopic Distal Attachment (AF-D series)May 30, 2025
K241679Disposable Cytology Brush (AF series)March 4, 2025
K241285Disposable Endoscope Valves Set (AF series)October 1, 2024
K231633Disposable Hemoclip (AF series)January 11, 2024
K230925Disposable Injection Needle AF seriesSeptember 27, 2023