Microvena Corp.
United StatesFDA applicant, unverified
- Devices
- 18
What Microvena Corp. makes
Microvena Corp. manufactures a range of interventional cardiology devices, including guidewires (such as the ULTRA-SELECT, HYTEK, and NINER NITINOL), thrombectomy tools (e.g., the AMPLATZ THROMBECTOMY DEVICE), and retrieval/snare systems (e.g., the GOOSE NECK SNARE and MICROSNARE). The portfolio also includes dilator needles (e.g., SOLOSTICK) and specialized catheters for vascular procedures.
All listed devices fall under Class II regulatory classification in the US and are authorised via 510(k) clearance through the FDA. The company’s products are registered under the US regulatory framework.
Catalogue
Search and filter all 18 devicesFrequently asked questions
How many devices does Microvena Corp. have in the registry?
The registry currently lists 18 devices for Microvena Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microvena Corp.'s devices?
Among its 18 most recently registered devices, Microvena Corp. has devices listed in FDA 510(k) (18 devices).
What risk classes do Microvena Corp.'s devices fall under?
Among its 18 most recently registered devices, the classes recorded for Microvena Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microvena Corp. in the registry?
The most recently registered devices listed for Microvena Corp. include ULTRA-SELECT GUIDEWIRE, HYTEK GUIDEWIRE, AMPLATZ THROMBECTOMY DEVICE(ATD 603, 602, 801, 802)/FOOT PEDAL ASSEMBLY(AK 200), CRICKET and SOLOSTICK (AMPLATZ DILATOR NEEDLE).