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ZuriMED Technologies AG

FDA Regulatory Profile

ZuriMED Technologies AG appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 2, 2026.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253867FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnitJanuary 2, 2026
K241219FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker InstruDecember 11, 2024

FDA data resources