The Korean company's BluEX expandable cervical interbody cage received a Special 510(k) clearance.
- Type
- FDA decision
- Company
- L&K Biomed
- Device
- BluEX Cervical Expandable Cage System
- Date
- 18 August 2026
- Jurisdiction
- US
- Classification
- 510(k) K262489 (ODP)
- Source
- FDA 510(k) database
Official source →Source checked