# Biomedical Diagnostics (Bmd) SA

- Location (FDA's records): Marne La Vallee Cedex 2, FR
- FDA decisions: 10 (2005–2010): 10 510(k) clearances
- Product codes: MOB (3), LLL (3), MST (1), JZO (1), LKO (1), LSW (1)
- Predicates its devices cite: 19 (4 its own); citations of its devices by later devices: 5 (4 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
- Elias U.S.A., Inc.: 6 (https://510kreport.com/company/elias-usa)
- Inova Diagnostics, Inc.: 3 (https://510kreport.com/company/inova-diagnostics)
- Sweden Diagnostics (Germany) GmbH: 3 (https://510kreport.com/company/sweden-diagnostics-germany)
- General Biometrics, Inc.: 2 (https://510kreport.com/company/general-biometrics)
- Pharmacia & Upjohn Co.: 1 (https://510kreport.com/company/pharmacia-upjohn)

## Firms that cite its devices most
- Inova Diagnostics, Inc.: 1 (https://510kreport.com/company/inova-diagnostics)

## Its most-cited devices
- K053653: Fidis Connective 10, Model MX006 (2006), cited by 2
- K071210: Modification to Fidis Connective 10*, Model MX006 (2007), cited by 1
- K053012: Fidis Vasculitis, Model MX007 (2006), cited by 1
- K070458: Modification to Fidis Vasculitis, Model MX007 (2007), cited by 1

## Recent decisions
- K102607: Fidistm Connective 10, Fidistm Analyzer, Caris (Dec 3, 2010)
- K100917: Fidis Vasculitis Assay Kit and Analyzer and Caris System (Nov 3, 2010)
- K070458: Modification to Fidis Vasculitis, Model MX007 (Dec 21, 2007)
- K071210: Modification to Fidis Connective 10*, Model MX006 (Dec 19, 2007)
- K061794: Fidis TM Thyro, Model MX002 (Nov 21, 2006)
- K060380: Fidis Dsdna (May 2, 2006)
- K053383: Fidis Celiac (Mar 29, 2006)
- K053653: Fidis Connective 10, Model MX006 (Mar 13, 2006)

Source page: https://510kreport.com/company/biomedical-diagnostics-bmd