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Pro3dure Medical GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231775GR Resin System MSIAugust 8, 2024
K212017Thermeo SystemApril 8, 2022
K211415GR Splint Resin SystemOctober 21, 2021
K210298GR-14 Resin SystemMay 5, 2021
K201827GR-17 Resin SystemNovember 5, 2020