# The Newman Group, LLC

- Location (FDA's records): Lake Bluff, IL
- FDA decisions: 2 (2006–2009): 2 510(k) clearances
- Product codes: ITX (1), KNG (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Newman Medical: 1 (https://510kreport.com/company/newman-medical)

## Its most-cited devices
- K090465: Digdop Ultrasound System (2009), cited by 1

## Recent decisions
- K090465: Digdop Ultrasound System (Apr 8, 2009)
- K061091: Babybeat Cordless (May 4, 2006)

Source page: https://510kreport.com/company/newman-group