Micro Therapeutics, Inc. D/B/A: Ev3, Inc.
Country not established
- Devices
- 1
What Micro Therapeutics, Inc. D/B/A: Ev3, Inc. makes
Micro Therapeutics, Inc. (d/b/a Ev3, Inc.) manufactures hydrophilic guidewires, including the SILVERSPEED, X-CELERATOR, X-PEDION, and MIRAGE series, designed for vascular and interventional procedures. These devices are intended for use in coronary and peripheral angiography, facilitating catheter navigation and exchange within blood vessels.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting their authorised status for commercial distribution in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micro Therapeutics, Inc. D/B/A: Ev3, Inc. have in the registry?
The registry currently lists 1 device for Micro Therapeutics, Inc. D/B/A: Ev3, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micro Therapeutics, Inc. D/B/A: Ev3, Inc.'s devices?
Among its 1 most recently registered device, Micro Therapeutics, Inc. D/B/A: Ev3, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Micro Therapeutics, Inc. D/B/A: Ev3, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Micro Therapeutics, Inc. D/B/A: Ev3, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micro Therapeutics, Inc. D/B/A: Ev3, Inc. in the registry?
The most recently registered devices listed for Micro Therapeutics, Inc. D/B/A: Ev3, Inc. include SILVERSPEED HYDROPHILIC GUIDEWIRE, X-CELERATOR HYDROPHILIC EXCHANGE GUIDEWIRE, X-PEDION HYDROPHILIC GUIDEWIRE, MIRAGE HY.