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Celularity Receives U.S. Food And Drug Administration (FDA) Preliminary Assessment For Celularity's Investigational Fuse Bone Void Filler To Be Regulated As A Device By FDA's Center For Devices And Radiological Health

Celularity’s Pre-Request for Designation is based on data demonstrating 100 percent biochemical characterization of the product Celularity intends to submit 510 pre-market notification to the. | April 3, 2023 ....

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Celularity Shares Climb 9.7% on FDA Agreement over Product Recommendation

Celularity Shares Climb 9.7% on FDA Agreement over Product Recommendation
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Celularity (CELU) Receives Preliminary Assessment of Product Classification and Jurisdiction for CTW to be Regulated as a Device

Celularity (CELU) Receives Preliminary Assessment of Product Classification and Jurisdiction for CTW to be Regulated as a Device
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