# Penrith Corporation

- Location (FDA's records): Plymouth Meeting, PA
- FDA decisions: 1 (2010–2010): 1 510(k) clearance
- Product codes: IYN (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (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
- Acuson Corp.: 1 (https://510kreport.com/company/acuson)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Philips Medical Systems, Inc.: 1 (https://510kreport.com/company/philips-medical-systems)

## Firms that cite its devices most
- Healcerion Co., Ltd.: 1 (https://510kreport.com/company/healcerion)
- Siemens Medi Cal Solutions, Inc.: 1 (https://510kreport.com/company/siemens-medi-cal-solutions)
- Guangzhou Sonostar Technologies Co., Ltd.: 1 (https://510kreport.com/company/guangzhou-sonostar-technologies)

## Its most-cited devices
- K100598: Penrith Elettra Ultrasound System (2010), cited by 3

## Recent decisions
- K100598: Penrith Elettra Ultrasound System (Nov 19, 2010)

Source page: https://510kreport.com/company/penrith