L and K Biomed Corporation Limited
South KoreaFDA applicant, unverified
- Devices
- 1
What L and K Biomed Corporation Limited makes
L and K Biomed Corporation Limited manufactures the ASK System, which is a spinal fixation device.
The company is based in the US, and its product is regulated as a Class II medical device listed in the FDA 510(k) registry.
Catalogue
ASK System Ref K181146
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does L and K Biomed Corporation Limited have in the registry?
The registry currently lists 1 device for L and K Biomed Corporation Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list L and K Biomed Corporation Limited's devices?
Among its 1 most recently registered device, L and K Biomed Corporation Limited has devices listed in FDA 510(k) (1 device).
What risk classes do L and K Biomed Corporation Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for L and K Biomed Corporation Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from L and K Biomed Corporation Limited in the registry?
The most recently registered devices listed for L and K Biomed Corporation Limited include ASK System.