Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K112787
›
Descendants
Devices descending from K112787
3 later devices reach Kerator through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K241183
ISO Abutment
Seum Medi Co., Ltd.
2025
0
—
+1
K173141
CSM Submerged3-L Implant System
Csm Implant
2018
0
—
+1
K132144
Kerator
LK Consulting Group USA, Inc.
2014
0
—