Fortimedix Surgical B.V.
NetherlandsFDA 510(k) applicant, unverified
- Devices
- 20
What Fortimedix Surgical B.V. makes
Fortimedix Surgical B.V. manufactures the FMX314 Surgical Platform, a reusable surgical device designed for minimally invasive procedures.
The FMX314 Surgical Platform is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 20 devicesCompany details
- DUNS number
- 492888563
- [email protected]
- Phone
- +31454047470
Frequently asked questions
How many devices does Fortimedix Surgical B.V. have in the registry?
The registry currently lists 20 devices for Fortimedix Surgical B.V.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fortimedix Surgical B.V.'s devices?
Among its 20 most recently registered devices, Fortimedix Surgical B.V. has devices listed in FDA 510(k) (1 device) and FDA GUDID (19 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Fortimedix Surgical B.V.'s devices fall under?
Among its 20 most recently registered devices, the classes recorded for Fortimedix Surgical B.V.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fortimedix Surgical B.V. in the registry?
The most recently registered devices listed for Fortimedix Surgical B.V. include symphonX™ Handle with on/off ratchet, symphonX™ Suction/Irrigation, symphonX™ Maryland short and symphonX™ Maryland.