Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K170171
›
Descendants
Devices descending from K170171
3 later devices reach IOLMaster 700 through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K191051
ARGOS
Santec Corporation
2019
0
—
+1
K173771
IOLMaster 700
Carl Zeiss Meditec, AG
2018
1
1
+2
K252633
Unity DX (Udx)
Cylite Pty., Ltd.
2025
0
—