# Rivanna Medical, Inc.

- Location (FDA's records): Charlottesville, VA
- FDA decisions: 8 (2014–2026): 8 510(k) clearances
- Names in FDA's records: Rivanna Medical, Inc. (6); Rivanna Medical, LLC (2)
- Product codes: IYO (6), ITX (2)
- 510(k) review time since 2016: median 120 days, against 139 for FDA's reviews in the same codes and years (5 of 7 faster)
- Predicates its devices cite: 10 (5 its own); citations of its devices by later devices: 6 (5 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
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- GE Medical Systems Ultrasound & Primary Care Diagnostics, LLC: 1 (https://510kreport.com/company/ge-medical-systems-ultrasound-primary-care-diagnostics)
- Verathon Incorporated: 1 (https://510kreport.com/company/verathon)
- Ardent Sound, Inc.: 1 (https://510kreport.com/company/ardent-sound)
- Mobisante, Inc.: 1 (https://510kreport.com/company/mobisante)

## Firms that cite its devices most
- Tissue Differentiation Intelligence, LLC: 1 (https://510kreport.com/company/tissue-differentiation-intelligence)

## Its most-cited devices
- K243937: Accuro 3S (2025), cited by 2
- K132736: Accuro 3000 Ultrasound Scanner (2014), cited by 2
- K250469: Accuro® 3S Needle Guide Kit (2025), cited by 1
- K171594: Accuro (2017), cited by 1

## Recent decisions
- K262093: Accuro XV (Oct 20, 2026)
- K253452: Accuro 3S (Jul 24, 2026)
- K261014: Accuro® 3S Needle Guide Kit (Jul 24, 2026)
- K254021: Accuro XV (Apr 9, 2026)
- K250469: Accuro® 3S Needle Guide Kit (Jun 13, 2025)
- K243937: Accuro 3S (May 23, 2025)
- K171594: Accuro (Oct 20, 2017)
- K132736: Accuro 3000 Ultrasound Scanner (Mar 11, 2014)

Source page: https://510kreport.com/company/rivanna-medical