Sweetbio, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sweetbio, Inc. has 2 FDA 510(k) cleared medical devices. Based in Memphis, US.
Last cleared in 2023. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sweetbio, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical as regulatory consultant.
2 devices