Axogen Corporation

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
12
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K231708Axoguard HA+ Nerve Protector (AGHA12); Axoguard HA+ Nerve Protector (AGHA22); Axoguard HA+ Nerve ProOctober 12, 2023
K223640Axoguard HA+ Nerve Protector (AGHA12); Axoguard HA+ Nerve Protector (AGHA22); Axoguard HA+ Nerve ProApril 7, 2023
K163446AxoGen Nerve CapAugust 8, 2017