Expanding Orthopedics, Inc. is one of 18425 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Expanding Orthopedics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FLXfit™, FLXFIT INTERVERTEBRAL BODY FUSION DEVICE, EOI SPINAL SYSTEM
3
Total
3
Cleared
0
Denied
Expanding Orthopedics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Philedelphia, US.
Historical record: 3 cleared submissions from 2009 to 2017. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Expanding Orthopedics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Technologies Corp. as regulatory consultant.
FDA 510(k) Regulatory Record - Expanding Orthopedics, Inc.
3 devices