Micrus Corp.
United StatesFDA applicant, unverified
- Devices
- 6
What Micrus Corp. makes
Micrus Corp. manufactures embolization coils and delivery systems designed for neurovascular and peripheral vascular applications, including microcoils for cerebral aneurysm treatment and stretch-resistant variants for enhanced stability. Their portfolio includes microcatheters and specialized coil systems tailored for precise vascular occlusion procedures.
The company’s devices are classified as Class II under FDA regulations and are authorised via 510(k) clearance. Products are listed in the FDA’s 510(k) database, reflecting compliance with US medical device regulations. The manufacturer operates from the United States.
Catalogue
Micrus Microcoil System Ref K032872
Regimes: 510(k) Registry: 510(k)Micrus Stretch-Resistant Microcoil System, MSR01 Ref K022420
Regimes: 510(k) Registry: 510(k)Micrus Microcatheter Ref K032624
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Micrus Microcoil Delivery System, MDS03 Ref K002056
Regimes: 510(k) Registry: 510(k)Micrus Modified Microcoil System, Cerecyte Ref K033813
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micrus Corp. have in the registry?
The registry currently lists 6 devices for Micrus Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micrus Corp.'s devices?
Among its 6 most recently registered devices, Micrus Corp. has devices listed in FDA 510(k) (6 devices).
What risk classes do Micrus Corp.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Micrus Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micrus Corp. in the registry?
The most recently registered devices listed for Micrus Corp. include MICRUS MICROCOIL SYSTEM, MICRUS STRETCH-RESISTANT MICROCOIL SYSTEM, MSR01, MICRUS MICROCATHETER and MICRUS MICROCOIL SYSTEMS, MODELS HEL, SPH, STR, FSR AND HSR.