Rhein'83 Srl

FDA Regulatory Profile

Rhein'83 Srl has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 9, 2018

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Rhein83
Same company group
0010—

Recent 510(k) Clearances

K-NumberDeviceDate
K171409OT EQUATORApr 9, 2018
K160382OT EQUATORAug 11, 2016
K142211OT EQUATORNov 25, 2015
K033630MODIFICATION OF: SPHERO FLEX, PIVOT FLEX, AND SPHERO BLOCKApr 21, 2004