Barosense, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Barosense, Inc. makes
Barosense, Inc. manufactures endoscopic stapling devices, including the ACE Stapler (Model F0031) and its associated cartridges for tissue approximation. The company also produces endogastric tubes and introducer bougies, such as the Barosense Endogastric Tube (Model F0034), designed for gastric applications.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The company is based in the United States.
Catalogue
Ace Stapler, Model F0031 Ref K082044
Regimes: 510(k) Registry: 510(k)Barosense Endogastric Tube And Introducer Bougie Ref K120126
Regimes: 510(k) Registry: 510(k)Ace Stapler And Cartridge Ref K120147
Regimes: 510(k) Registry: 510(k)Barosense Endogastric Tube (Egt), Model F0034 Ref K082589
Regimes: 510(k) Registry: 510(k)Ace Stapler And Cartridge Ref K110829
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Barosense, Inc. have in the registry?
The registry currently lists 5 devices for Barosense, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barosense, Inc.'s devices?
Among its 5 most recently registered devices, Barosense, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Barosense, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Barosense, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Barosense, Inc. in the registry?
The most recently registered devices listed for Barosense, Inc. include ACE STAPLER, MODEL F0031, BAROSENSE ENDOGASTRIC TUBE AND INTRODUCER BOUGIE, ACE STAPLER AND CARTRIDGE and BAROSENSE ENDOGASTRIC TUBE (EGT), MODEL F0034.