Micrus Endovascular Corporation
United StatesFDA applicant, unverified
- Devices
- 23
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Micrus Endovascular Corporation makes
Micrus Endovascular Corporation makes microcoil systems, microcatheters, guide wires, and occlusion balloon catheters for endovascular procedures. Specific products include the Cashmere-Cerecyte and Cashmere-SR microcoil systems, DeltaPlush microcoil system, Ascent occlusion balloon catheter, Courier and Courier Enzo microcatheters, Watusi guide wire, and various microcoil delivery systems.
The devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 23 devicesFDA recalls
FDA recall records list 1 recall initiated by Micrus Endovascular Corporation, initiated on 2006-09-08. By recorded status: 1 terminated. The reasons filed fall into these groups: mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2006
- 8 Sep 2006 Z-1542-06 Unclassified (pre-2012) Terminated During use, the introducer may cause the guide wire''s coating to strip off and may result in loose material which could break free and enter the blood stream.
Frequently asked questions
How many devices does Micrus Endovascular Corporation have in the registry?
The registry currently lists 23 devices for Micrus Endovascular Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micrus Endovascular Corporation's devices?
Among its 23 most recently registered devices, Micrus Endovascular Corporation has devices listed in FDA 510(k) (23 devices).
What risk classes do Micrus Endovascular Corporation's devices fall under?
Among its 23 most recently registered devices, the classes recorded for Micrus Endovascular Corporation's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Micrus Endovascular Corporation?
FDA recall records list 1 recall initiated by Micrus Endovascular Corporation, the most recent initiated on 8 Sep 2006. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Micrus Endovascular Corporation in the registry?
The most recently registered devices listed for Micrus Endovascular Corporation include MICRUS MICROCOIL SYSTEM CASHMERE-CERECYTE, MODEL CRC; CASHMERE-SR, MODEL SRC, MICRUS MICROCOLI SYSTEM, DELTAPLUSH, MODELS CPL, DPL, MICRUS ASCENT OCCLUSION BALLOON CATHETER and MICRUS MICROCOIL SYSTEM, CASHMERE MODEL SRC.