Baebies, Inc. is one of 16326 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baebies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FINDER Flu A&B/SARS-CoV-2 Test, FINDER G6PD
3
Total
2
Cleared
1
Denied
Baebies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Durham, US.
Latest FDA clearance: Sep 2026. Active since 2017.
Browse the FDA 510(k) cleared devices submitted by Baebies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Baebies, Inc.
3 devices