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Alton

Alton (Shanghai) Medical Instruments Co., Ltd. · Model AF-D2423JZR-7 · UDI-DI 06975543352012

PKL
10
510(k) clearances
7,146
Adverse events (25 deaths)
6
Recalls
54
Facilities

Recalls

DateFirmReason
2026-03-03Wilson-Cook Medical Inc.Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
2023-05-04Olympus Corporation of the AmericasComplaints on clip deployment occurring during clinical procedures, leading to hazardous situations where clips fail to achieve their expected function or deploy incorrectly, poten
2023-05-04Olympus Corporation of the AmericasComplaints on clip deployment occurring during clinical procedures, leading to hazardous situations where clips fail to achieve their expected function or deploy incorrectly, poten
2023-05-04Olympus Corporation of the AmericasComplaints on clip deployment occurring during clinical procedures, leading to hazardous situations where clips fail to achieve their expected function or deploy incorrectly, poten
2023-05-04Olympus Corporation of the AmericasComplaints on clip deployment occurring during clinical procedures, leading to hazardous situations where clips fail to achieve their expected function or deploy incorrectly, poten
2019-02-04US Endoscopy Group IncPotential esophageal laceration during a patient procedure

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.