W.R. Grace & Co.-Conn. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
W.R. Grace & Co.-Conn. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
W.R. Grace & Co.-Conn. has 2 FDA 510(k) cleared medical devices. Based in Lexington, US.
Historical record: 2 cleared submissions from 1986 to 1987. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by W.R. Grace & Co.-Conn. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - W.R. Grace & Co.-Conn.
2 devices