Axogen Corporation
Axogen Corporation appears in FDA public data with 0 recalls, 3 510(k) clearances, 13 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 12, 2023.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 13
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K231708 | Axoguard HA+ Nerve Protector (AGHA12); Axoguard HA+ Nerve Protector (AGHA22); Axoguard HA+ Nerve Pro | October 12, 2023 |
| K223640 | Axoguard HA+ Nerve Protector (AGHA12); Axoguard HA+ Nerve Protector (AGHA22); Axoguard HA+ Nerve Pro | April 7, 2023 |
| K163446 | AxoGen Nerve Cap | August 8, 2017 |