Common Sense, Ltd.
Country not established
- Devices
- 2
What Common Sense, Ltd. makes
Common Sense, Ltd. manufactures the VS-SENSE TEST, a diagnostic device used for specific clinical assessments, and the AMNISCREEN HOME DETECTION LINER KIT, designed for at-home monitoring of amniotic fluid levels during pregnancy.
The company’s products fall under Class I medical devices and are listed via FDA 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Vs-Sense Test Ref K091287
Regimes: 510(k) Registry: 510(k)Amniscreen Home Detection Liner Kit Ref K071100
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Common Sense, Ltd. have in the registry?
The registry currently lists 2 devices for Common Sense, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Common Sense, Ltd.'s devices?
Among its 2 most recently registered devices, Common Sense, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Common Sense, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Common Sense, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Common Sense, Ltd. in the registry?
The most recently registered devices listed for Common Sense, Ltd. include VS-SENSE TEST and AMNISCREEN HOME DETECTION LINER KIT.