B. Bruan Surgical, SA
SpainFDA 510(k) applicant, unverified
- Devices
- 1
What B. Bruan Surgical, SA makes
B. Braun Surgical, SA manufactures the Lyograft, a medical device designed for surgical applications, including tissue integration and wound management solutions.
The Lyograft 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
Lyograft Ref K192452
510(k) 510(k)
Frequently asked questions
How many devices does B. Bruan Surgical, SA have in the registry?
The registry currently lists 1 device for B. Bruan Surgical, SA. Devices recorded under merged duplicate company entries are counted once.
Which registries list B. Bruan Surgical, SA's devices?
Among its 1 most recently registered device, B. Bruan Surgical, SA has devices listed in FDA 510(k) (1 device).
What risk classes do B. Bruan Surgical, SA's devices fall under?
Among its 1 most recently registered device, the classes recorded for B. Bruan Surgical, SA's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from B. Bruan Surgical, SA in the registry?
The most recently registered devices listed for B. Bruan Surgical, SA include Lyograft.