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Stuckenbrock Medizintechnik GmbH

FDA Regulatory Profile

Stuckenbrock Medizintechnik GmbH appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 29, 2018.

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K171624IXOS Radius Plate SystemMarch 29, 2018
K171628HBS2 Headless Bone ScrewJanuary 12, 2018
K042902HERBERT ULNAR HEAD PROSTHESIS SYSTEMDecember 27, 2004

FDA data resources