Medifield Medical Co., Ltd.
South KoreaFDA applicant, unverified FDA FEI 3033519208
- Devices
- 181
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Medifield Medical Co., Ltd. makes
Medifield Medical Co., Ltd. manufactures the Montblanc Plate System, a medical device designed for internal fixation in orthopedic surgery, used to stabilize bone fractures through plate and screw constructs.
The Montblanc Plate System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Search and filter all 181 devicesShowing 1-50 of 181
Company details
- FDA FEI number
- 3033519208
- DUNS number
- 695956893
- Address
- 94-40, Yongjeonggyeongje-ro 1-gil, Gunnae-myeon, Pocheon-si, Gyeonggi-do, Pocheon Gyeonggi
- [email protected]
- Phone
- +821089806787
Frequently asked questions
How many devices does Medifield Medical Co., Ltd. have in the registry?
The registry currently lists 181 devices for Medifield Medical Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medifield Medical Co., Ltd.'s devices?
Among its 50 most recently registered devices, Medifield Medical Co., Ltd. has devices listed in FDA GUDID (50 devices).
What risk classes do Medifield Medical Co., Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Medifield Medical Co., Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medifield Medical Co., Ltd. in the registry?
The most recently registered devices listed for Medifield Medical Co., Ltd. include Tray for Montblanc Radius Plate System MF002, Montblanc Depth Gauge RFM059, Montblanc Depth Gauge RFM010 and Montblanc Driver Shaft RFM004.