Biopsybell S.A.S.
Country not established
- Devices
- 3
What Biopsybell S.A.S. makes
Biopsybell S.A.S. manufactures biopsy-related devices, including the SPEEDYBELL, EASYBELL, and OSTEOBELL. These products are designed for use in medical procedures requiring precise tissue sampling or bone biopsy applications, such as orthopedic or diagnostic evaluations.
The company’s portfolio is classified under FDA’s Class II medical devices and is listed in the 510(k) premarket notification registry. These devices are regulated under the United States’ medical device framework, ensuring compliance with applicable safety and performance standards.
Catalogue
Speedybell Ref K010735
Regimes: 510(k) Registry: 510(k)Easybell Ref K011075
Regimes: 510(k) Registry: 510(k)Osteobell Ref K011104
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biopsybell S.A.S. have in the registry?
The registry currently lists 3 devices for Biopsybell S.A.S.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biopsybell S.A.S.'s devices?
Among its 3 most recently registered devices, Biopsybell S.A.S. has devices listed in FDA 510(k) (3 devices).
What risk classes do Biopsybell S.A.S.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Biopsybell S.A.S.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biopsybell S.A.S. in the registry?
The most recently registered devices listed for Biopsybell S.A.S. include SPEEDYBELL, EASYBELL and OSTEOBELL.