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# FDA Clears 3D Manufacturer’s Cervical Interbody Device
- URL: https://www.fdaweb.com/fda-clears-3d-manufacturers-cervical-interbody-device/
- Published: 2021-02-03T12:00:00.000Z
- Updated: 2026-09-14T16:45:07.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5148590

FDA has cleared an NGMedical 510(k) for its 3D-manufactured titanium cervical interbody BEE cage implant. The device is designed to reduce the risk of subsidence while allowing fusion, the company says. Its honeycomb structure allows for bony ingrowth and it demonstrates the reduced use of titanium to minimize risks of X-ray artifacts, while offering a large graft space, it says.