Sientra, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Sientra, Inc. has 3 FDA 510(k) cleared medical devices. Based in Santa Barbara, US.
Last cleared in 2023. Active since 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sientra, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Sientra, Inc.
3 devices