Porex Technologies Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Porex Technologies Corp. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Porex Technologies Corp. has 2 FDA 510(k) cleared medical devices. Based in Fairburn, US.
Historical record: 2 cleared submissions from 1992 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Porex Technologies Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Porex Technologies Corp.
2 devices