Medical Device Manufacturer · US , Tampa , FL

Axiom Worldwide, Inc. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001

Recent clearances: DRX9000 TRUE SPINAL DECOMPRESSION SYSTEM, AXIOM NVP8500, AXIOM EPS8000

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Axiom Worldwide, Inc. Physical Medicine ✕

4 devices

1-4 of 4

Cleared May 26, 2006

DRX9000 TRUE SPINAL DECOMPRESSION SYSTEM

Physical Medicine · 67d

Cleared Aug 11, 2005

Physical Medicine · 100d

Cleared Jul 28, 2005

Physical Medicine · 133d

Cleared May 01, 2001

Physical Medicine · 90d

Data Source

Sourced from the FDA 510(k) public files . 176,325 total devices indexed.

Last updated: Sep 26, 2026