Tokos Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Tokos Medical Corp. makes
Tokos Medical Corp. manufactures uterine activity monitoring devices, including the TERM GUARD 5000 and TERM GUARD II, designed to track contractions during pregnancy.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Term Guard 5000 Uterine Activity Ref K843011
Regimes: 510(k) Registry: 510(k)Term Guard Ii Device Ref K893770
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tokos Medical Corp. have in the registry?
The registry currently lists 2 devices for Tokos Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tokos Medical Corp.'s devices?
Among its 2 most recently registered devices, Tokos Medical Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tokos Medical Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tokos Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tokos Medical Corp. in the registry?
The most recently registered devices listed for Tokos Medical Corp. include TERM GUARD 5000 UTERINE ACTIVITY and TERM GUARD II DEVICE.