# Axiom Usa., Inc.

- Location (FDA's records): Tampa, FL
- FDA decisions: 4 (2002–2003): 4 510(k) clearances
- Product codes: ITH (2), NHN (2)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 5 (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
- Nor-Am Patient Care Products, Inc.: 2 (https://510kreport.com/company/nor-am-patient-care-products)
- Axiom Worldwide, Inc.: 1 (https://510kreport.com/company/axiom-worldwide)
- Vat-Tech, Inc.: 1 (https://510kreport.com/company/vat-tech)
- The Saunders Group: 1 (https://510kreport.com/company/saunders-group)
- Andi Electromedical Aps: 1 (https://510kreport.com/company/andi-electromedical)
- Microlight Corporation of America: 1 (https://510kreport.com/company/microlight-of-america)

## Firms that cite its devices most
- Excite Medical of Tampa Bay, LLC: 1 (https://510kreport.com/company/excite-medical-of-tampa-bay)
- Axiom Worldwide, Inc.: 1 (https://510kreport.com/company/axiom-worldwide)
- Integra Life Sciences: 1 (https://510kreport.com/company/integra-life-sciences)
- Cert Health Sciences, LLC: 1 (https://510kreport.com/company/cert-health-sciences)
- North American Medical Corp (Nam): 1 (https://510kreport.com/company/north-american-medical-nam)

## Its most-cited devices
- K023160: DRX5000 (2002), cited by 4
- K022602: DRX3000 (2003), cited by 1

## Recent decisions
- K033015: Axiom Biolaser LLLT Series-3 (Nov 25, 2003)
- K030622: Axiom Biolaser LLLT Series-1 (Sep 9, 2003)
- K022602: DRX3000 (Jan 23, 2003)
- K023160: DRX5000 (Dec 20, 2002)

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