Timpel S.A. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Timpel S.A. has 3 FDA 510(k) cleared medical devices. Based in Sao Paulo, BR.
Latest FDA clearance: Sep 2025. Active since 2022. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Timpel S.A. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Timpel S.A.
3 devices