Perflex is one of 492 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Perflex - FDA 510(k) Cleared Devices
Recent clearances: Acryfree Denture Base Material and Biosens Denture Base Material
1
Total
1
Cleared
0
Denied
Perflex has 1 FDA 510(k) cleared medical devices. Based in Netanya, IL.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Perflex Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Licensale, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Perflex
1 devices