Timpel, Inc. is one of 50 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Timpel, Inc. - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Timpel, Inc. has 0 FDA 510(k) cleared medical devices. Based in Sao Paulo-Sp, BR.
Active since 2018. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Timpel, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Timpel, Inc.
1 devices