Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
DEN210013
›
Descendants
Devices descending from DEN210013
2 later devices reach OsteoProbe through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K221195
OsteoProbe
Active Life Scientific, Inc.
2022
1
—
+2
K250216
OsteoProbe (OP-100)
Active Life Scientific, Inc.
2025
0
—