Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K122768
›
Descendants
Devices descending from K122768
4 later devices reach Genesis through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K151485
Genesis
Dornier Medtech America, Inc.
2015
1
—
+1
K133434
Genesis II
Dornier Medtech America, Inc.
2014
2
—
+1
K130729
Extra Corporeal Shockwave Lithotripter
Dornier Medtech Systems
2013
0
—
+2
K220871
Nautilus
Dornier Medtech America, Inc.
2022
0
—