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Enrollment Completed in BIOMAG™-LL Clinical Study Evaluating Longer Lengths for Freesolve™ Resorbable Magnesium Scaffold

Key Takeaway: Teleflex Incorporated has announced the successful completion of patient enrollment in the BIOMAG™-LL Clinical Study. This study evaluates the safety and clinical performance of the Freesolve™ Resorbable Magnesium Scaffold in lengths of 35 mm and 40 mm for treating de novo coronary lesions. The study aims to enhance clinical evidence for this innovative medical technology.

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POSITIVE FACTORS

  • Successful completion of patient enrollment in the study.
  • Evaluation of new lengths for the Freesolve™ Resorbable Magnesium Scaffold.
  • Commitment to expanding clinical evidence for innovative medical technologies.

Full Press Release Details

WAYNE, Pa.--(BUSINESS WIRE)--Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced the successful completion of patient enrollment in the BIOMAG™-LL Clinical Study, evaluating the safety and clinical performance of the Freesolve™ Resorbable Magnesium Scaffold (RMS) in 35 mm and 40 mm lengths for the treatment of de novo coronary lesions up to 38 mm. The study reflects Teleflex's commitment to expanding clinical evidence supporting the use of the F

Frequently Asked Questions

What is the BIOMAG-LL Clinical Study?

The BIOMAG-LL Clinical Study evaluates the safety and performance of the Freesolve™ Resorbable Magnesium Scaffold.

What lengths are being evaluated in the study?

The study evaluates the Freesolve™ Resorbable Magnesium Scaffold in 35 mm and 40 mm lengths.

What is the purpose of the Freesolve™ Scaffold?

The Freesolve™ Scaffold is designed for the treatment of de novo coronary lesions up to 38 mm.

Who announced the completion of enrollment?

Teleflex Incorporated announced the successful completion of patient enrollment.

Last updated: Oct 12, 2026