Medentika GmbH

FDA Regulatory Profile

Medentika GmbH appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 23, 2025.

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253341Custom Abutments ASDec 23, 2025
K242542Medentika CAD/CAM AbutmentsApr 22, 2025
K223113Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBases, Medentika Multi-uApr 15, 2024
K201711CARES Screw - Retained Bars and Bridges (SRBB)Dec 8, 2020
K200906MINICONE ImplantOct 16, 2020
K191123Multi-unit AbutmentsJan 6, 2020
K180564Medentika Abutment System, Medentika CAD/CAM Abutments, Medentika CAD/CAM TiBasesJan 7, 2019
K170838Medentika CAD/CAM TiBasesSep 15, 2017
K150203Medentika CAD/CAM AbutmentsOct 23, 2015
K142167MEDENTIKA ABUTMENT SYSTEMFeb 20, 2015