The Teleflex Freesolve RMS uses magnesium alloy and bioabsorbable coating technology to provide vessel support during and after implantation.

Teleflex Interventional President and GM Jason Fontana discusses the breakthrough Freesolve RMS and the resorbable technology ...

Teleflex, a Wayne, Pennsylvania-based medical technology company, has received a U.S. Food and Drug Administration (FDA) ...

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Teleflex is currently evaluating Freesolve in the BIOMAG-III Pivotal Trial to support a future premarket approval application.

The 35 mm and 40 mm scaffold lengths evaluated in BIOMAG™-LL Clinical Study are designed to complement the current Freesolve™ RMS size matrix, which offers diameters of 2.5 mm, 3.0 mm, 3.5 mm and 4.0 ...

The Freesolve Resorbable Magnesium Scaffold previously received the same designation for below-the-knee interventions. This update covers minimally invasive coronary procedures.

Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation (BDD) ...

ⓘ This article is third-party content and does not represent the views of this site. We make no guarantees regarding its accuracy or completeness. 102 patients enrolled across 14 European centers to ...

Teleflex Incorporated announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Device Designation (BDD) for its Freesolve? Resorbable Magnesium Scaffold (RMS) for ...

WAYNE, Pa.--(BUSINESS WIRE)--Oct. 22, 2026-- Teleflex Incorporated (NYSE: TFX), a leading global provider of medical technologies, today announced that the U.S. Food and Drug Administration (FDA) has ...

ⓘ This article is third-party content and does not represent the views of this site. We make no guarantees regarding its accuracy or completeness. Teleflex Incorporated (NYSE: TFX), a leading global ...