Cellah Medical Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 1
What Cellah Medical Co., Ltd. makes
Cellah Medical Co., Ltd. manufactures the BLESSING System, a medical device designed for minimally invasive spinal procedures, including the placement of interbody fusion cages and instrumentation.
The BLESSING System is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance pathway. The company is based in the United States.
Catalogue
BLESSING System Ref K243176
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cellah Medical Co., Ltd. have in the registry?
The registry currently lists 1 device for Cellah Medical Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cellah Medical Co., Ltd.'s devices?
Among its 1 most recently registered device, Cellah Medical Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cellah Medical Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cellah Medical Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cellah Medical Co., Ltd. in the registry?
The most recently registered devices listed for Cellah Medical Co., Ltd. include BLESSING System.