• Regentis recently received European regulatory approval for a next-generation GelrinC manufacturing process that increases production yield by 400%.
• The company is advancing commercialization through scalable manufacturing, surgeon training programs, and continued U.S. Phase III clinical progress.
• These developments reinforce Regentis’ strategy of bringing innovative cartilage repair technology from clinical validation to commercial scale, with unit economics that improve as production volumes build.

Regentis Biomaterials Ltd. (NYSE American: RGNT) is advancing GelrinC, its innovative cell-free hydrogel implant for focal knee cartilage repair, with a value proposition that extends across the entire healthcare ecosystem. Designed to simplify treatment while improving clinical outcomes, GelrinC offers meaningful benefits for surgeons, patients, and healthcare payers alike. Recent European regulatory approval for a next-generation solvent-free manufacturing process, which boosts production yield by approximately 400%, strengthens the company’s ability to deliver a practical, scalable solution that addresses longstanding limitations in cartilage repair at a much lower production cost.

Unlike complex cell-based therapies or temporary treatment approaches such as microfracture, GelrinC is designed as an off-the-shelf solution. The ready-to-use hydrogel is delivered during a single procedure lasting roughly 10 minutes, cures in situ, and gradually resorbs as the patient’s own cells regenerate durable, hyaline-like cartilage. This combination of procedural…

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NOTE TO INVESTORS: The latest news and updates relating to RGNT are available in the company’s newsroom at https//ibn.fm/RGNT

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This contant was orignally distributed by InvestorBrandNetwork (IBN). Blockchain Registration, Verification & Enhancement provided by NewsRamp™. The source URL for this press release is Surgeon, Payer, Patient Win: The Economic and Workflow Advantages Positioning GelrinC as a New Standard of Care for Knee Cartilage Repair.