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Stryker Craniomaxillofacial

FDA Regulatory Profile

Stryker Craniomaxillofacial 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 Jan 13, 2024.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K232350Stryker Facial iD SystemJan 13, 2024
K092743THE LEIBINGER ADVANCE INTERNAL MIDFACE DISTRACTION SYSTEMJan 15, 2010
K070876STRYKER TWIST DRILLSApr 27, 2007

FDA data resources