Adri/Technam is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Adri/Technam - FDA 510(k) Cleared Devices
3
Total
2
Cleared
0
Denied
Adri/Technam has 2 FDA 510(k) cleared medical devices. Based in Park Forest, US.
Historical record: 2 cleared submissions from 1991 to 2000. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Adri/Technam Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Adri/Technam
3 devices