Rivanna Medical, Inc.

FDA Regulatory Profile

Rivanna Medical, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 24, 2026.

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253452Accuro 3SJuly 24, 2026
K261014Accuro® 3S Needle Guide KitJuly 24, 2026
K254021Accuro XVApril 9, 2026
K250469Accuro® 3S Needle Guide KitJune 13, 2025
K243937Accuro 3SMay 23, 2025
K171594AccuroOctober 20, 2017
K132736ACCURO 3000 ULTRASOUND SCANNERMarch 11, 2014