Home › Device types › MOF
Guide, Wire, Catheter, Neurovasculature
FDA product code MOF · Class 2 · Cardiovascular
165
Registered devices
670
Adverse events
2
Recalls
45
510(k) clearances
Devices with this code
Aristotle — SCIENTIA VASCULAR LLCCHIKAI Nexus petit — ASAHI INTECC CO., LTD.CHIKAI Nexus 014 — ASAHI INTECC CO., LTD.Synchro SELECT — Stryker CorporationWillow 14 Guidewire — Arbor Endovascular LLCWaveSelect — Enlight Medical Technologies(Shenzhen) Co., Ltd.DCwire™ — Shanghai Achieva Medical Suzhou Co., Ltd.AGILITY — Cerenovus, Inc.Synchro SELECT — Stryker CorporationAristotle — SCIENTIA VASCULAR LLCDCwire™ — Shanghai Achieva Medical Suzhou Co., Ltd.Ikon 14 Guidewire — IMPERATIVE CARE, INC.Willow 14 Guidewire — Arbor Endovascular LLCWillow 14 Guidewire — Arbor Endovascular LLCAristotle — SCIENTIA VASCULAR LLCWillow 14 Guidewire — Arbor Endovascular LLCSynchro2 — Stryker CorporationMirageTM — Micro Therapeutics, Inc.DCwire™ — Shanghai Achieva Medical Suzhou Co., Ltd.Aristotle — SCIENTIA VASCULAR LLCCHIKAI — ASAHI INTECC CO., LTD.RADIFOCUS — Terumo Medical Products (Hangzhou) Co., Ltd.pORTAL® EXT Extension Wire — PHENOX LIMITEDHYBRID Guidewire — BALT USA LLC
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.