Medical Device Manufacturer · US , Avon , MA

Ranfac Corporation - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2019

Recent clearances: Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA), Ran-Flex-B Bone Marrow Aspiration Needle, J-Type Marrow Biopsy Needle,T-Type Marrow Biopsy Needle,Tweezer Bone Marrow Biopsy Needle,

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) Regulatory Record - Ranfac Corporation

4 devices
1-4 of 4
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