Machina Medical, Inc.
United Statesfrom the FDA registration address FDA FEI 3045158005
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Machina Medical, Inc. makes
Machina Medical, Inc. manufactures the MFUSE (MS001), a medical device designed for vascular access procedures, including the creation of arteriovenous (AV) fistulas and grafts.
The MFUSE is classified as a Class II device under FDA regulations and has been authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
- Registry: GUDID
Mfuse (MS001) Ref K250319
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3045158005
- Address
- 1007 Mansell Rd Ste A-107, Roswell, GA, 30076
Frequently asked questions
How many devices does Machina Medical, Inc. have in the registry?
The registry currently lists 2 devices for Machina Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Machina Medical, Inc.'s devices?
Among its 2 most recently registered devices, Machina Medical, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What are the newest devices from Machina Medical, Inc. in the registry?
The most recently registered devices listed for Machina Medical, Inc. include MFUSE MS001 and MFUSE (MS001).