# Femspec LLC

- Location (FDA's records): Port Townsend, WA
- FDA decisions: 4 (2004–2006): 4 510(k) clearances
- Product codes: HIB (2), HHK (1), PCF (1)
- Predicates its devices cite: 1 (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 whose devices it cites most
- Doctor'S Research Group, Inc.: 1 (https://510kreport.com/company/doctor-s-research-group)

## Firms that cite its devices most
- Femasys, Inc.: 1 (https://510kreport.com/company/femasys)

## Its most-cited devices
- K060320: Femecc Endocervical Curette (2006), cited by 1

## Recent decisions
- K060320: Femecc Endocervical Curette (Jul 28, 2006)
- K052192: Femspce-S Disposable Sterile Vaginal Speculum, Model ST-I (Feb 2, 2006)
- K051294: Femtest Endometrial Suction Curette, Model FT-1 (Dec 21, 2005)
- K041757: Femspec Disposable Vaginal Speculum (Dec 23, 2004)

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