Mark Abramson, D.D.S., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mark Abramson, D.D.S., Inc. - FDA 510(k) Cleared Devices
Recent clearances: OASYS Oral/Nasal Airway System and OASYS Herbst with Dentitrac Patient Monitor
2
Total
2
Cleared
0
Denied
Mark Abramson, D.D.S., Inc. has 2 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 2 cleared submissions from 2003 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Mark Abramson, D.D.S., Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Fishermed Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mark Abramson, D.D.S., Inc.
2 devices