/PRNewswire/ The "Acellular Dermal Matrix Implant Market - A Global and Regional Analysis - Analysis and Forecast, 2024-2030" report has been added to.
By Ben Glickman MiMedx Group said on Friday it received an FDA warning letter related to the classification of its product Axiofill. The regulator has reaffirmed that the company s treatment.
MiMedx Group said on Friday
it had received a warning letter from the U.S. Food and Drug
Administration related to the classification of its
placental-derived tissue product Axiofill, and its shares.