Tempus Wins FDA Approval for xT CDx, Expanding Solid Tumor Testing Portfolio
Tempus has received US FDA approval for its tumor-only xT CDx, becoming the first laboratory with companion diagnostic approval for both tumor-only and tumor-normal genomic profiling.
ACL Injury | 30/05/2026 | By News Bureau | 123
Miach Orthopaedics’ BEAR Implant becomes the first sports medicine device to carry an FDA-cleared claim for lowering long-term osteoarthritis risk compared with traditional ACL reconstruction.
ACL Injury | 16/01/2026 | By News Bureau | 474
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