Home › Device types › MOF
Guide, Wire, Catheter, Neurovasculature
FDA product code MOF · Class 2 · Cardiovascular
150
Registered devices
657
Adverse events
2
Recalls
43
510(k) clearances
Devices with this code
Synchro SELECT — Stryker CorporationNEUROSCOUT — Medos International SàrlCHIKAI — ASAHI INTECC CO., LTD.Synxess — Enlight Medical Technologies(Shenzhen) Co., Ltd.Ikon 14 Guidewire — IMPERATIVE CARE, INC.Aristotle — SCIENTIA VASCULAR LLCWillow 14 Guidewire — Arbor Endovascular LLCHYBRID Guidewire — BALT USA LLCAGILITY — Cerenovus, Inc.Cypress 14 Guidewire — Arbor Endovascular LLCIkon 14 Pro Guidewire — IMPERATIVE CARE, INC.CHIKAI black — ASAHI INTECC CO., LTD.HYBRID Guidewire — BALT USA LLCIkon 18 Pro Guidewire — IMPERATIVE CARE, INC.CHIKAI Nexus 014 — ASAHI INTECC CO., LTD.Volo — SCIENTIA VASCULAR LLCCHIKAI Nexus petit — ASAHI INTECC CO., LTD.Willow 14 Guidewire — Arbor Endovascular LLCIkon 24 Guidewire — IMPERATIVE CARE, INC.Aristotle — SCIENTIA VASCULAR LLCCypress 14 Guidewire — Arbor Endovascular LLCVolo — SCIENTIA VASCULAR LLCWillow 14 Guidewire — Arbor Endovascular LLCCHIKAI Nexus 014 — ASAHI INTECC CO., LTD.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-18 | Stryker Neurovascular | Stryker Neurovascular has observed an increased frequency of PTFE coating damage occurring on the Synchro Guidewires that may be caused by the practice of backl |
| 2017-08-07 | Microvention, Inc. | There is a potential for the hydrophilic coating on the guidewire to delaminate from the guidewire. |
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