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Merit Medical Systems (MMSI) FDA Approvals

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Merit Medical Systems' Drug in the FDA Approval Process

This section highlights FDA-related milestones and regulatory updates for drugs developed by Merit Medical Systems (MMSI). Over the past two years, Merit Medical Systems has reported clinical trial outcomes, regulatory submissions, approvals, and other FDA events for drugs and therapies such as WRAPSODY. For definitions of regulatory abbreviations such as NDA, BLA, or PDUFA, see the event status legend.

WRAPSODY FDA Regulatory Events

WRAPSODY is a drug developed by Merit Medical Systems for the following indication: Cell-Impermeable Endoprosthesis (CIE). This drug is under review by the U.S. Food and Drug Administration (FDA). Below is a timeline of key regulatory milestones for this therapy.

Merit Medical Systems FDA Events - Frequently Asked Questions

As of now, Merit Medical Systems (MMSI) has not received any FDA approvals for its therapy in the last two years.

In the past two years, Merit Medical Systems (MMSI) has reported FDA regulatory activity for WRAPSODY.

The most recent FDA-related event for Merit Medical Systems occurred on August 18, 2025, involving WRAPSODY. The update was categorized as "Enrollment Update," with the company reporting: "Merit Medical Systems announced today the successful enrollment of the first patient in the WRAP North America registry."

Currently, Merit Medical Systems has one therapy (WRAPSODY) targeting the following condition: Cell-Impermeable Endoprosthesis (CIE)..

More FDA Event Resources from MarketBeat

  • NDA: New Drug Application
  • ANDA: Abbreviated New Drug Application
  • sNDA: Supplemental New Drug Application
  • BLA: Biologics License Application
  • sBLA: Supplemental Biologics License Application
  • FDA Approved: Approved by the FDA
  • EMA: European Medicines Agency
  • CE Mark: European Union Certification
  • NMPA: China National Medical Products Administration
  • MHLW: Japanese Ministry of Health
  • FDA Meeting: Consultation with FDA
  • Pre-IND: Pre-Investigational New Drug Meeting
  • Breakthrough Therapy: Special FDA designation for promising therapies
  • Fast Track: Accelerated FDA approval pathway
  • Orphan Drug: Designation for rare disease treatments
  • RPD: Rare Pediatric Disease Designation
  • RMAT: Regenerative Medicine Advanced Therapy
  • DSMB Review: Data Safety Monitoring Board Review
  • IDMC Review: Independent Data Monitoring Committee
  • MAA: MHRA Marketing Authorization Application
  • RTF: Refusal to File (Rejected Application)
  • 510(k): FDA Clearance for Medical Devices
  • Rolling Submission: Staggered regulatory review process

This page (NASDAQ:MMSI) was last updated on 8/21/2025 by MarketBeat.com Staff
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