# Inverness Medical Professional Diagnostics

- Location (FDA's records): Scarborough, ME
- FDA decisions: 1 (2007–2007): 1 510(k) clearance
- Product codes: MJH (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- Binax, Inc.: 1 (https://510kreport.com/company/binax)

## Firms that cite its devices most
- Ssi Diagnostica A/S: 1 (https://510kreport.com/company/ssi-diagnostica-a-s)

## Its most-cited devices
- K070522: Modification to: Binax Now  Legionella Urinary Antigen Test, #852-000,852-012 (2007), cited by 1

## Recent decisions
- K070522: Modification to: Binax Now  Legionella Urinary Antigen Test, #852-000,852-012 (Mar 15, 2007)

Source page: https://510kreport.com/company/inverness-medical-professional-diagnostics