Sweetbio, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sweetbio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: APIS (R), VERIS (TM), Apis
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.
Regulatory submissions have been managed by Kapstone Medical, LLC and Kapstone Medical.
FDA 510(k) Regulatory Record - Sweetbio, Inc.
2 devices