Timpel S.A. is one of 50 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Timpel S.A. - FDA 510(k) Cleared Devices
Recent clearances: Enlight 2100 (TPL-E2103-0), Enlight 2100, Enlight 2100
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.
FDA 510(k) Regulatory Record - Timpel S.A.
3 devices