Allotrope Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Allotrope Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: StimSite
1
Total
1
Cleared
0
Denied
Allotrope Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Allotrope Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Allotrope Medical, Inc.
1 devices