MiMedx says US FDA's warning letter for Axiofill not related to safety
Dec 29 (Reuters) - MiMedx Group MDXG.O said on Friday the U.S. Food and Drug Administration's warning letter for its recently launched placental-derived tissue product Axiofill was not related to safety. (Reporting by Sriparna Roy in Bengaluru; Editing by Shounak Dasgupta) ((Sriparna.Roy@thomsonreuters.com))
Recent news on MiMedx
See all newsBrief: Mimedx Announces Favorable Federal Court Ruling In Axiofill® Regulatory Classification Matter
MiMedx Group Inc reports results for the quarter ended June 30 - Earnings Summary
Brief: Mimedx To Acquire Sanara Medtech
MiMedx Q2 sales fall less than expected; set to acquire Sanara MedTech
Brief: MiMedx Q2 Sales USD 64.362 Million Vs. IBES Estimate USD 63.5 Million