Celestray Biotech Company, LLC., FDA Approvals

0 new drug approvals and 2 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	What it is	Route	Decided
Rebuilder Nerve Guidance Conduit510(k)Jan 29, 2024Neurology	Neurology	510(k)Substantially Equivalent (Traditional)	Jan 29, 2024
SpinMedix Absorbable Fibrous Membrane510(k)Jul 6, 2023General, Plastic Surgery	General, Plastic Surgery	510(k)Substantially Equivalent (Traditional)	Jul 6, 2023