# Biospace Med

- Location (FDA's records): Washington, DC
- FDA decisions: 4 (2007–2011): 4 510(k) clearances
- Product codes: LLZ (3), KPR (1)
- Predicates its devices cite: 13 (3 its own); citations of its devices by later devices: 11 (3 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Siemens Medical Solutions USA, Inc.: 2 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Agfa Healthcare N.V.: 2 (https://510kreport.com/company/agfa-healthcare)
- Lodox Systems (Pty), Ltd.: 1 (https://510kreport.com/company/lodox-systems)
- Toshiba America Medical Systems, In.C: 1 (https://510kreport.com/company/toshiba-america-medical-systems-in-c)
- General Electrical Espanola, S.A.: 1 (https://510kreport.com/company/general-electrical-espanola)
- Philips Medical Systems North America, Inc.: 1 (https://510kreport.com/company/philips-medical-systems-north-america)
- Cgr Medical Corp.: 1 (https://510kreport.com/company/cgr-medical)
- Eastman Kodak Company: 1 (https://510kreport.com/company/eastman-kodak)

## Firms that cite its devices most
- Eos Imaging: 8 (https://510kreport.com/company/eos-imaging)

## Its most-cited devices
- K080529: Stereos Workstation (2008), cited by 4
- K090050: Stereos Workstation (2010), cited by 3
- K071546: EOS (2007), cited by 2
- K101398: Stereos Workstation (2011), cited by 2

## Recent decisions
- K101398: Stereos Workstation (Feb 4, 2011)
- K090050: Stereos Workstation (Mar 5, 2010)
- K080529: Stereos Workstation (Aug 29, 2008)
- K071546: EOS (Sep 18, 2007)

Source page: https://510kreport.com/company/biospace-med