Free Flow Medical, Inc.
United StatesFDA 510(k) applicant, unverified FDA FEI 3015925639
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Free Flow Medical, Inc. makes
Free Flow Medical, Inc. manufactures the LungFlow Basket Catheter, a device designed for bronchoscopic procedures to remove obstructions or foreign bodies from the airways.
The company’s portfolio is regulated under Class II medical devices in the United States, with the LungFlow Basket Catheter authorised via the FDA’s 510(k) pathway. The manufacturer is based in the US.
Catalogue
LungFlow Airway Catheter Ref K254037
510(k) 510(k)LungFlow Basket Catheter Ref K254040
510(k) 510(k)
Company details
- FDA FEI number
- 3015925639
- Address
- 44380 S. Grimmer Blvd., Fremont, CA, 94538
Frequently asked questions
How many devices does Free Flow Medical, Inc. have in the registry?
The registry currently lists 2 devices for Free Flow Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Free Flow Medical, Inc.'s devices?
Among its 2 most recently registered devices, Free Flow Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Free Flow Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Free Flow Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Free Flow Medical, Inc. in the registry?
The most recently registered devices listed for Free Flow Medical, Inc. include LungFlow Airway Catheter and LungFlow Basket Catheter.