# Dermaport, Inc.

- Location (FDA's records): Santa Clarita, CA
- FDA decisions: 2 (2007–2009): 2 510(k) clearances
- Product codes: MSD (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (1 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
- Medical Components, Inc.: 1 (https://510kreport.com/company/medical-components)
- Med-Conduit, Inc.: 1 (https://510kreport.com/company/med-conduit)

## Its most-cited devices
- K071202: Dermaport Percutaneous Vascular Access System (Pvas) (2007), cited by 1

## Recent decisions
- K091760: Dermaport Ported Vascular Access System (Pvas) (Jul 20, 2009)
- K071202: Dermaport Percutaneous Vascular Access System (Pvas) (Nov 30, 2007)

Source page: https://510kreport.com/company/dermaport