# Ultrafem, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (1993–1997): 2 510(k) clearances
- Product codes: HHE (2)
- Predicates its devices cite: 0 (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 that cite its devices most
- Eastmed, Inc.: 1 (https://510kreport.com/company/eastmed)

## Its most-cited devices
- K971303: Instead, Softcup (1997), cited by 1

## Recent decisions
- K971303: Instead, Softcup (Jun 6, 1997)
- K920792: Softcup (TM):2 (Oct 5, 1993)

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