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Aesculap Implants Systems, LLC

FDA Regulatory Profile

Aesculap Implants Systems, LLC has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 13, 2023

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances4Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K231769activL® Next Generation InstrumentationJul 13, 2023
K172235CoreHip® SystemMar 28, 2018
K172032Modulift Vertebral Body Replacement (VBR) SystemNov 20, 2017
K143443VEGA Knee System, Columbus Total Knee SystemMar 25, 2015

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.