Axiom Worldwide, Inc. is one of 24178 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Axiom Worldwide, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DRX9000 TRUE SPINAL DECOMPRESSION SYSTEM, AXIOM NVP8500, AXIOM EPS8000
4
Total
4
Cleared
0
Denied
Axiom Worldwide, Inc. has 4 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 4 cleared submissions from 2001 to 2006. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Axiom Worldwide, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Axiom Worldwide, Inc.
4 devices