# Axiom Worldwide, Inc.

- Location (FDA's records): Tampa, FL
- FDA decisions: 4 (2001–2006): 4 510(k) clearances
- Product codes: IPF (2), ITH (2)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Axiom Usa., Inc.: 1 (https://510kreport.com/company/axiom-usa)
- Vax-D Medical Technologies USA, L.C.: 1 (https://510kreport.com/company/vax-d-medical-technologies-usa-lc)

## Firms that cite its devices most
- Axiom Usa., Inc.: 1 (https://510kreport.com/company/axiom-usa)
- Integrity Life Sciences: 1 (https://510kreport.com/company/integrity-life-sciences)
- Excite Medical of Tampa Bay, LLC: 1 (https://510kreport.com/company/excite-medical-of-tampa-bay)
- North American Medical Corp (Nam): 1 (https://510kreport.com/company/north-american-medical-nam)

## Its most-cited devices
- K060735: DRX9000 True Spinal Decompression System (2006), cited by 3
- K010292: DRX 2000 (2001), cited by 1

## Recent decisions
- K060735: DRX9000 True Spinal Decompression System (May 26, 2006)
- K051135: Axiom NVP8500 (Aug 11, 2005)
- K050687: Axiom EPS8000 (Jul 28, 2005)
- K010292: DRX 2000 (May 1, 2001)

Source page: https://510kreport.com/company/axiom-worldwide