# Duopross Meditech Corporate

- Location (FDA's records): Farmingdale, NY
- FDA decisions: 1 (2025–2025): 1 510(k) clearance
- Product codes: FMF (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (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
- Us Infusion Inc. D/B/A Truecare Biomedix-USA: 1 (https://510kreport.com/company/us-infusion-d-b-a-truecare-biomedix-usa)

## Recent decisions
- K252518: DuoprossTM Smart Cap (Type I) (Dec 17, 2025)

Source page: https://510kreport.com/company/duopross-meditech-corporate