Medical Device Manufacturer · BR , Sao Paulo

Timpel S.A. - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2022
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.

3 devices
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All3 Anesthesiology 3