Fossa Medical, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Fossa Medical, Inc. makes
Fossa Medical, Inc. manufactures ureteral open stents and ureteral open lumen stents, which are designed for urinary tract applications. The company also produces modifications to ureteral stone sweepers, a tool used in the removal of kidney stones.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Fossa Ureteral Open Stents Ref K072293
510(k) 510(k)Fossa Ureteral Open Lumen Stent Ref K033368
510(k) 510(k)Modification To Fossa Ureteral Stone Sweeper Ref K031292
510(k) 510(k)
Frequently asked questions
How many devices does Fossa Medical, Inc. have in the registry?
The registry currently lists 3 devices for Fossa Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fossa Medical, Inc.'s devices?
Among its 3 most recently registered devices, Fossa Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Fossa Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Fossa Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fossa Medical, Inc. in the registry?
The most recently registered devices listed for Fossa Medical, Inc. include FOSSA URETERAL OPEN STENTS, FOSSA URETERAL OPEN LUMEN STENT and MODIFICATION TO FOSSA URETERAL STONE SWEEPER.