Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K211415
›
Descendants
Devices descending from K211415
2 later devices reach GR Splint Resin System through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K231775
GR Resin System MSI
Pro3Dure Medical
2024
0
—
+1
K232448
FREEPRINT® splintmaster
Detax GmbH
2023
0
—