Aerobine, Inc. is one of 20637 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aerobine, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DENTAL HANDPIECES, MODELS: KARAM STD/MINI
1
Total
1
Cleared
0
Denied
Aerobine, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Aerobine, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Aerobine, Inc.
1 devices