Spiration, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Spiration, Inc. makes
Spiration, Inc. manufactures medical devices including the B7 2C Occlusion Balloon, Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator, Flexible 19G EBUS Needle, ViziShot FLEX, and PeriFLEX, which are specialized tools used in various endoscopic and surgical procedures.
The company's portfolio consists of Class II devices listed in the FDA 510(k) registry, and Spiration, Inc. is based in the United States.
Catalogue
B7 2C Occlusion Balloon Ref K171492
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Flexible 19G EBUS Needle Ref K142909
Regimes: 510(k) Registry: 510(k)ViziShot FLEX Ref K152922
Regimes: 510(k) Registry: 510(k)PeriFLEX Ref K162611
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Spiration, Inc. have in the registry?
The registry currently lists 5 devices for Spiration, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Spiration, Inc.'s devices?
Among its 5 most recently registered devices, Spiration, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Spiration, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Spiration, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Spiration, Inc. in the registry?
The most recently registered devices listed for Spiration, Inc. include B7 2C Occlusion Balloon, Active Needle Endoscopic Treatment (ANET) Electrosurgical Applicator, Flexible 19G EBUS Needle and ViziShot FLEX.