Laurane Medical SAS
FranceFDA applicant, unverified
- Devices
- 1
What Laurane Medical SAS makes
Laurane Medical Sas manufactures bone marrow biopsy kits, including the OmniBone™ Bone Marrow Biopsy Kit with Power Driver and the OmniBone™ Bone Biopsy Kit with Power Driver. These devices are designed for obtaining bone marrow samples, incorporating power-driven systems to assist in the biopsy procedure.
The company’s portfolio is regulated under Class II devices in the US and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver Ref K230015
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laurane Medical Sas have in the registry?
The registry currently lists 1 device for Laurane Medical Sas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laurane Medical Sas's devices?
Among its 1 most recently registered device, Laurane Medical Sas has devices listed in FDA 510(k) (1 device).
What risk classes do Laurane Medical Sas's devices fall under?
Among its 1 most recently registered device, the classes recorded for Laurane Medical Sas's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laurane Medical Sas in the registry?
The most recently registered devices listed for Laurane Medical Sas include OmniBone™ Bone Marrow Biopsy Kit with Power Driver, OmniBone™ Bone Biopsy Kit with Power Driver.