Carbon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carbon, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DB 4000 High Impact Denture Base
1
Total
1
Cleared
0
Denied
Carbon, Inc. has 1 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Carbon, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Nilo Medical Consulting Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Carbon, Inc.
1 devices