Fortifier International Co., Ltd.
TaiwanFDA 510(k) applicant, unverified
- Devices
- 1
What Fortifier International Co., Ltd. makes
Fortifier International Co., Ltd. manufactures the Fortifier Digital Wrist Blood Pressure Monitor (Model LF-01), a non-invasive device designed for home or clinical use to measure systolic and diastolic blood pressure via the wrist.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- 510(k) 510(k)
Frequently asked questions
How many devices does Fortifier International Co., Ltd. have in the registry?
The registry currently lists 1 device for Fortifier International Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fortifier International Co., Ltd.'s devices?
Among its 1 most recently registered device, Fortifier International Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Fortifier International Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fortifier International Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fortifier International Co., Ltd. in the registry?
The most recently registered devices listed for Fortifier International Co., Ltd. include FORTIFIER DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LF-01.