Apteryx, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Apteryx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: XVWeb 3D
3
Total
3
Cleared
0
Denied
Apteryx, Inc. has 3 FDA 510(k) cleared medical devices. Based in Akron, US.
Historical record: 3 cleared submissions from 1998 to 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Apteryx, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Apteryx, Inc.
3 devices