Arkis Biosciences Inc.
Country not established
- Devices
- 12
What Arkis Biosciences Inc. makes
Arkis Biosciences Inc. manufactures the SureFlo External Ventricular Drainage (EVD) Catheter, a device used for draining cerebrospinal fluid from the brain in medical settings.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Search and filter all 12 devicesCompany details
- DUNS number
- 078846878
- [email protected]
- Phone
- +1(800)654-2873
Frequently asked questions
How many devices does ARKIS BIOSCIENCES INC. have in the registry?
The registry currently lists 12 devices for ARKIS BIOSCIENCES INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ARKIS BIOSCIENCES INC.'s devices?
Among its 12 most recently registered devices, ARKIS BIOSCIENCES INC. has devices listed in FDA 510(k) (1 device) and FDA GUDID (11 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ARKIS BIOSCIENCES INC.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for ARKIS BIOSCIENCES INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from ARKIS BIOSCIENCES INC. in the registry?
The most recently registered devices listed for ARKIS BIOSCIENCES INC. include Subcutaneous Guidewire - Medium 41.240.502, Precision Tunneler - Large 41.020.503, Precision Tunneler - Small 41.020.501 and CerebroFlo EVD Catheter Set 37.550.101.