Cousin Biotech S.A.R.L.
Country not established
- Devices
- 1
What Cousin Biotech S.A.R.L. makes
Cousin Biotech S.A.R.L manufactures BIOMESH P1, a synthetic mesh for surgical reinforcement, as well as BIOMESH Plug and Patch, designed for tissue repair and defect closure in medical procedures.
These products are classified as Class II devices under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Biomesh P1 And Biomesh Plug And Patch Ref K002479
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cousin Biotech S.A.R.L have in the registry?
The registry currently lists 1 device for Cousin Biotech S.A.R.L. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cousin Biotech S.A.R.L's devices?
Among its 1 most recently registered device, Cousin Biotech S.A.R.L has devices listed in FDA 510(k) (1 device).
What risk classes do Cousin Biotech S.A.R.L's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cousin Biotech S.A.R.L's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cousin Biotech S.A.R.L in the registry?
The most recently registered devices listed for Cousin Biotech S.A.R.L include BIOMESH P1 AND BIOMESH PLUG AND PATCH.