# Artemis Medical, Inc.

- Location (FDA's records): Haywayd, CA
- FDA decisions: 3 (2001–2003): 3 510(k) clearances
- Product codes: FZP (2), KNW (1)
- Predicates its devices cite: 7 (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
- United States Surgical, A Division of Tyco Healthc: 2 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Imagyn Surgical: 1 (https://510kreport.com/company/imagyn-surgical)
- Biopsys Medical, Inc.: 1 (https://510kreport.com/company/biopsys-medical)
- Ethicon Endo-Surgery, Inc.: 1 (https://510kreport.com/company/ethicon-endo-surgery)
- Neothermia Corp.: 1 (https://510kreport.com/company/neothermia)
- Endocare, Inc.: 1 (https://510kreport.com/company/endocare)

## Firms that cite its devices most
- Focal Therapeutics: 1 (https://510kreport.com/company/focal-therapeutics)

## Its most-cited devices
- K032217: 14G Cormark Biopsy Site Identifier (2003), cited by 1

## Recent decisions
- K032217: 14G Cormark Biopsy Site Identifier (Aug 21, 2003)
- K020024: Caris Minitome Biopsy Instrument (Apr 3, 2002)
- K003777: Caris Site Marker (Mar 6, 2001)

Source page: https://510kreport.com/company/artemis-medical