Ranfac Corporation - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Ranfac Corporation has 4 FDA 510(k) cleared medical devices. Based in Avon, US.
Last cleared in 2023. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Ranfac Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Ranfac Corporation
4 devices
Cleared
Feb 21, 2023
Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA)
General & Plastic Surgery
78d
Cleared
Sep 18, 2020
Ran-Flex-B Bone Marrow Aspiration Needle
General & Plastic Surgery
37d
Cleared
Jun 12, 2019
J-Type Marrow Biopsy Needle,T-Type Marrow Biopsy Needle,Tweezer Bone Marrow...
General & Plastic Surgery
131d
Cleared
Apr 25, 2019
Ranfac Cartilage Biopsy Needle
General & Plastic Surgery
163d