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Icotec AG FDA Approvals
0 new drug approvals and 8 device clearances on file. This applicant is not matched to a listed company.
Newest first
A new drug approval is an original application; a 510(k) is a device shown equivalent to one already sold.
| Product |
|---|
| CMORE® CT System; CMORE® CT System Navigated Instruments510(k)Nov 12, 2025Orthopedic |
| VADER® Pedicle System and VADER®one Pedicle System510(k)Feb 27, 2025Orthopedic |
| icotec Anterior Cervical Plate System510(k)May 17, 2024Orthopedic |
| icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurn TLIF Lumbar Cage)510(k)Apr 5, 2024Orthopedic |
| KONG®-TL VBR System and KONG® C VBR System510(k)Apr 4, 2024Orthopedic |
| VADER® Pedicle System510(k)Feb 26, 2024Orthopedic |
| VADER® Pedicle System Navigated Instruments510(k)Jun 27, 2023Neurology |
| VADER® Pedicle System, G21 Cement510(k)Jan 9, 2023Orthopedic |