Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K211443
›
Descendants
Devices descending from K211443
2 later devices reach Aibolit 3D+ through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K232339
Augmented Reality Application
Sira Medical, Inc.
2024
0
—
+1
K222458
Aibolit 3D+
Aibolit Technologies, LLC
2023
0
—