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NanoHive Medical, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K254105Hive™ Standalone Cervical System and Hive™ C Interbody SystemFebruary 13, 2026
K231241NanoHive Medical Lumbar Interbody SystemJuly 12, 2023
K223190Hive™ Standalone Cervical SystemDecember 12, 2022