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VS3-IR

VISIONSENSE LTD. · Model 153-0055 · UDI-DI 10884521816701

OWNGCJ Prescription
1
510(k) clearances
1,630
Adverse events (1 deaths)
4
Recalls
69
Facilities

Description

153-0055 VS3 IR ENDOSCOPE 5MM 0DEG

Recalls

DateFirmReason
2024-09-24Olympus Corporation of the AmericasDoes not meet the requirements for electromagnetic compatibility (EMC) of the standard IEC 60601-1-2. Electromagnetic interference occurring during a procedure may cause the devic
2022-10-17Visionsense, Ltd.Broken Optical fiber cable damage can occur through handling or bending and can lead to loss of functionality and heating/melting of the outer cable surface.
2022-10-17Visionsense, Ltd.XXX
2022-10-17Visionsense, Ltd.Broken Optical fiber cable damage can occur through handling or bending and can lead to loss of functionality and heating/melting of the outer cable surface.

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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.