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Rivanna Medical, Inc.

FDA Regulatory Profile

Rivanna Medical, Inc. has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Oct 20, 2026

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances8Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K262093Accuro XVOct 20, 2026
K261014Accuro® 3S Needle Guide KitJul 24, 2026
K253452Accuro 3SJul 24, 2026
K254021Accuro XVApr 9, 2026
K250469Accuro® 3S Needle Guide KitJun 13, 2025
K243937Accuro 3SMay 23, 2025
K171594AccuroOct 20, 2017
K132736ACCURO 3000 ULTRASOUND SCANNERMar 11, 2014

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.