Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K162321
›
Descendants
Devices descending from K162321
2 later devices reach EasyClip Xpress through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K210582
EasyClip® and EasyClip® Xpress
Stryker GmbH
2022
1
—
+2
K241932
OSSIOfiber® Compression Staple
OSSIO, Ltd.
2024
0
—