Etex Corporation
FDA Regulatory Profile
Etex Corporation appears in FDA public data with 0 recalls, 5 510(k) clearances, 6 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 18, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 6
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K243609 | EquivaBone Osteoinductive Bone Graft Substitute (EquivaBone ) | Dec 18, 2024 |
| K182107 | CarriGen PF | Aug 31, 2018 |
| K132868 | CARRICELL | Feb 20, 2015 |
| K141245 | ETEX MIXING AND DELIVERY SYSTEM | Jul 9, 2014 |
| K102812 | GAMMA-BSM; BETA-BSM; EQUIVABONE | Dec 3, 2010 |