S. Cordero Co. is one of 9 FDA 510(k) medical device manufacturers from Mexico in the dataset, ranked by real submission volume.
S. Cordero Co. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
S. Cordero Co. has 1 FDA 510(k) cleared medical devices. Based in Mexico City Cp 01030, MX.
Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by S. Cordero Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - S. Cordero Co.
1 devices