Mizuho America, Inc.
Mizuho America, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2022, with 4 FDA device recalls on record.
Top product codes for Mizuho America, Inc.
FDA recalls by Mizuho America, Inc.
- Z-0566-2021 — Microsurgical Operating Room Tables;7300B (18-350-70);
- Z-0567-2021 — Microsurgical Operating Room Tables;7300BX (18-351-70).
- Z-0377-2014 — Mizuho Sugita Titanium Standard Aneurysm Clip II , Temporary and permanent occlusion of cervical segment of cerebral aneurysms and peripheral blood vessels. They are designed for Single Use.
- Z-0378-2014 — Mizuho Sugita Titanium Standard Aneurysm Clip II , Temporary Mini Type No 58 Temporary and permanent occlusion of cervical segment of cerebral aneurysms and peripheral blood vessels. They are designed for Single Use.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Mizuho America, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.