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.
510(k) submissions have been managed by ProMedic Consulting, LLC as regulatory consultant.
3 devices