# Aframe Digital, Inc.

- Location (FDA's records): Reston, VA
- FDA decisions: 2 (2009–2012): 2 510(k) clearances
- Product codes: DRG (1), KMI (1)
- 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
- Telemedcare Pty, Ltd.: 1 (https://510kreport.com/company/telemedcare)
- Care Electronics, Inc.: 1 (https://510kreport.com/company/care-electronics)

## Firms that cite its devices most
- CSA Medical, Inc.: 1 (https://510kreport.com/company/csa-medical)
- Intel-Ge Care Innovations, LLC: 1 (https://510kreport.com/company/intel-ge-care-innovations)
- Centauri Medical, Inc.: 1 (https://510kreport.com/company/centauri-medical)
- Wireless Medcare, LLC: 1 (https://510kreport.com/company/wireless-medcare)

## Its most-cited devices
- K090138: Mobilecare Monitor, Model 2100 (2009), cited by 4

## Recent decisions
- K122333: Mobilecare Monitor (Nov 19, 2012)
- K090138: Mobilecare Monitor, Model 2100 (Apr 24, 2009)

Source page: https://510kreport.com/company/aframe-digital