Press Releases August 20, 2026 08:30 AM

Orchestra BioMed to Participate in the Wells Fargo 21st Annual Healthcare Conference

Orchestra BioMed to present at Wells Fargo Healthcare Conference highlighting pivotal trials and breakthrough device designations

By Derek Hwang
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Orchestra BioMed Holdings, Inc., a biomedical company focused on innovative medical device therapies, announced that its CEO will present at the Wells Fargo 21st Annual Healthcare Conference. The company is advancing two flagship products, AVIM Therapy for hypertension and the Virtue Sirolimus AngioInfusion Balloon, both of which have received FDA Breakthrough Device Designations and are currently in pivotal clinical trials. Orchestra BioMed has a strategic collaboration with Medtronic to develop and commercialize AVIM Therapy targeting a large patient population with uncontrolled hypertension.

Orchestra BioMed to Participate in the Wells Fargo 21st Annual Healthcare Conference
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Key Points

  • Orchestra BioMed will present at the major Wells Fargo Healthcare Conference, increasing investor visibility.
  • The company is developing two flagship biomedical products with FDA Breakthrough Device Designations: AVIM Therapy for hypertension and Virtue SAB for arterial disease.
  • Strategic collaboration with Medtronic enhances development and commercialization prospects for AVIM Therapy, targeting a significant market in patients with uncontrolled hypertension.

NEW HOPE, Pa., Aug. 20, 2026 (GLOBE NEWSWIRE) -- Orchestra BioMed Holdings, Inc. (Nasdaq: OBIO, “Orchestra BioMed” or the “Company”), a biomedical company accelerating high-impact technologies to patients through risk-reward sharing partnerships, today announced that Chairman and CEO David Hochman will present at the Wells Fargo 21st Annual Healthcare Conference on Thursday, Sept. 10, 2026 at 1:30pm ET and will also host one-on-one meetings with investors that day and on Wednesday, Sept. 9.

A live webcast of the event will be accessible through Orchestra BioMed’s Investor Relations website and will be available for replay following the event.

About Orchestra BioMed
Orchestra BioMed is a biomedical innovation company accelerating high-impact technologies to patients through strategic collaborations with market-leading global medical device companies. The Company’s two flagship product candidates - Atrioventricular Interval Modulation (AVIM) Therapy and Virtue® Sirolimus AngioInfusion™ Balloon (Virtue SAB) - are currently undergoing pivotal clinical trials for their lead indications, each representing multi-billion-dollar annual global market opportunities. AVIM Therapy is a bioelectronic treatment for hypertension, the leading risk factor for death worldwide, and is designed to be delivered by a pacemaker and achieve immediate, substantial and sustained reductions in blood pressure in patients with hypertensive heart disease. The Company has a strategic collaboration with Medtronic, one of the largest medical device companies in the world and the global leader in cardiac pacing therapies, for the development and commercialization of AVIM Therapy for the treatment of uncontrolled hypertension in pacemaker-indicated patients. AVIM Therapy has FDA Breakthrough Device Designations for these patients, as well as an estimated 7.7 million total patients in the U.S. with uncontrolled hypertension despite medical therapy and increased cardiovascular risk. Virtue SAB is a highly differentiated, first-of-its-kind non-coated drug delivery angioplasty balloon system designed to deliver a large liquid dose of proprietary extended-release formulation of sirolimus, SirolimusEFR™, for the treatment of atherosclerotic artery disease, the leading cause of mortality worldwide. Virtue SAB has been granted Breakthrough Device Designation by the FDA for the treatment of coronary in-stent restenosis, coronary small vessel disease and below-the-knee peripheral artery disease. For further information about Orchestra BioMed, please visit www.orchestrabiomed.com, and follow us on LinkedIn.

Investor Contact:
Silas Newcomb
Orchestra BioMed
[email protected]

Media Contact:
Nina Premutico
Orchestra BioMed
[email protected]


Risks

  • Outcomes of pivotal clinical trials are uncertain and could affect product approval and commercialization timelines.
  • Regulatory approvals, despite Breakthrough Device Designation, are not guaranteed and could delay market entry.
  • Dependence on collaboration with Medtronic means financial and operational risks if partnership dynamics change.

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