# Diagnostic Devices, Inc.

- Location (FDA's records): Deer Field, IL
- FDA decisions: 5 (2006–2009): 5 510(k) clearances
- Names in FDA's records: Diagnostic Devices, Inc. (4); Diagnostic Devices Pty, Ltd. (1)
- Product codes: NBW (3), DXH (1), CAF (1)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 7 (1 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
- Taidoc Technology Corporation: 2 (https://510kreport.com/company/taidoc-technology)
- Card Guard Scientific Survival, Ltd.: 1 (https://510kreport.com/company/card-guard-scientific-survival)
- Omron Healthcare, Inc.: 1 (https://510kreport.com/company/omron-healthcare)
- Health & Life Co., Ltd.: 1 (https://510kreport.com/company/health-life)

## Firms that cite its devices most
- Ok Biotech Co., Ltd.: 2 (https://510kreport.com/company/ok-biotech)
- Prodigy Diabetes Care, LLC: 2 (https://510kreport.com/company/prodigy-diabetes-care)
- Biotest Medical Corp.: 1 (https://510kreport.com/company/biotest-medical)
- Taidoc Technology Corporation: 1 (https://510kreport.com/company/taidoc-technology)

## Its most-cited devices
- K073118: Prodigy Voice Blood Glucose Monitoring System (2008), cited by 4
- K060467: Prodigy Blood Glucose Test System (2006), cited by 2
- K053593: Prodigy (2006), cited by 1

## Recent decisions
- K090307: Ddi Ultrasonic Nebulizer System (Jun 18, 2009)
- K073118: Prodigy Voice Blood Glucose Monitoring System (Mar 5, 2008)
- K072385: Heartevent, Model at (Jan 11, 2008)
- K060467: Prodigy Blood Glucose Test System (Jul 13, 2006)
- K053593: Prodigy (Jul 6, 2006)

Source page: https://510kreport.com/company/diagnostic-devices