B&Medi Co., Ltd.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 1
What B&Medi Co., Ltd. makes
B&Medi Co., Ltd. manufactures the Bio-MEM Ti Reinforced Membrane, a reinforced biomembrane designed for surgical applications requiring enhanced durability and tissue integration.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the U.S. regulatory database. The manufacturer is based in the United States.
Catalogue
Bio-MEM Ti Reinforced Membrane Ref K210797
510(k) 510(k)
Frequently asked questions
How many devices does B&Medi Co., Ltd. have in the registry?
The registry currently lists 1 device for B&Medi Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list B&Medi Co., Ltd.'s devices?
Among its 1 most recently registered device, B&Medi Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do B&Medi Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for B&Medi Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from B&Medi Co., Ltd. in the registry?
The most recently registered devices listed for B&Medi Co., Ltd. include Bio-MEM Ti Reinforced Membrane.