# Eastmed, Inc.

- Location (FDA's records): Dundas, CA
- FDA decisions: 2 (2008–2009): 2 510(k) clearances
- Product codes: HHW (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 4 (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
- Johnson & Johnson Medical, Inc.: 2 (https://510kreport.com/company/johnson-johnson-medical)
- Ultrafem, Inc.: 1 (https://510kreport.com/company/ultrafem)
- Deschutes Medical Products, Inc.: 1 (https://510kreport.com/company/deschutes-medical-products)

## Firms that cite its devices most
- Cntrl+, Inc.: 1 (https://510kreport.com/company/cntrl)
- Watkins-Conti Products, Inc.: 1 (https://510kreport.com/company/watkins-conti-products)
- Resilia, Inc.: 1 (https://510kreport.com/company/resilia)

## Its most-cited devices
- K081385: Uresta Pessary (2008), cited by 3
- K083769: Modification to Uresta Pessary (2009), cited by 1

## Recent decisions
- K083769: Modification to Uresta Pessary (Jan 14, 2009)
- K081385: Uresta Pessary (Oct 9, 2008)

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