Nephros Receives FDA 510(k) Clearance for HDF Assist Module
Nephros, Inc. (Nasdaq: NEPH) announced FDA 510(k) clearance for its HDF Assist Module, the first device in the U.S. to provide hemodiafiltration therapy for End-Stage Renal Disease patients. This milestone allows Nephros to enhance treatment options for patients without needing new, expensive equipment. The module will be piloted in select dialysis clinics to establish operational procedures and train staff. Nephros aims to improve water safety through innovative technology, serving both healthcare and commercial sectors.
- FDA clearance for HDF Assist Module opens new treatment paths for ESRD patients.
- Module allows existing dialysis machines to provide hemodiafiltration without significant investment in new equipment.
- Initial pilot program to establish procedures and train staff enhances operational readiness.
- Market acceptance of the HDF Assist Module remains uncertain.
- Dependence on third-party manufacturers poses potential operational risks.
- SRP lacks extensive experience in commercializing new technologies.
The First and Only FDA-Cleared Device Available in the United States to Provide Hemodiafiltration Therapy to Dialysis Patients
SOUTH ORANGE, NJ, May 17, 2022 (GLOBE NEWSWIRE) -- via NewMediaWire – Nephros, Inc. (Nasdaq: NEPH), a leading water technology company providing filtration and pathogen detection solutions to the medical and commercial markets, today announced that it has received FDA 510(k) clearance for its patented, second-generation HDF Assist Module. The HDF Assist Module is the first and only device in the United States cleared to provide hemodiafiltration (HDF) therapy to patients with End-Stage Renal Disease (ESRD).
“Receiving 510(k) clearance is truly a milestone moment for Nephros and Specialty Renal Products (SRP), our majority-owned subsidiary. Nephros was founded with the goal of providing solutions for patients with ESRD, and today is a big step forward in the process,” said Andy Astor, President and Chief Executive Officer of both Nephros and SRP. “The receipt of FDA clearance for our HDF Assist Module enables us to provide ESRD patients with a new therapeutic option.”
“Our HDF Assist Module is an innovation that offers practitioners the opportunity to use an existing hemodialysis (HD) machine to provide HDF therapy without the purchase of a new, costly machine,” continued Mr. Astor. “SRP’s Director of Commercial Operations, David Lee, an engineer and dialysis nurse with many years of clinical operations responsibility, will lead our initial focus on piloting the HDF Assist Module within select dialysis clinics.”
“Our first goal in any given dialysis clinic will be to support the development of internal procedures for operation of the HDF Assist Module, and the training of personnel to seamlessly execute those procedures,” said Mr. Lee. “Once the procedures are established and tested within the select clinics, we will then be able to work with additional clinics to roll out HDF as a therapeutic option for more dialysis patients.”
About Nephros
Nephros, Inc. is a company committed to improving the human relationship with water through leading, accessible technology. We provide innovative filtration and pathogen detection as part of an integrated approach to water safety that combines science, solutions, and support services. Nephros products serve the needs of customers within the healthcare and commercial markets, offering both proactive and emergency responses for water management.
For more information about Nephros, please visit nephros.com.
About Specialty Renal Products
Specialty Renal Products, Inc. (SRP) is a development-stage company focused on the advancement of hemodiafiltration (HDF) technology for patients with End-Stage Renal Disease (ESRD). SRP is committed to commercializing the second-generation Nephros HDF Assist Module to enable hemodialysis machines to also provide hemodiafiltration therapy.
Forward-Looking Statements
This release contains forward-looking statements that are subject to various risks and uncertainties. Such statements include statements regarding the anticipated market acceptance of the HDF Assist Module, Nephros’ and SRP’s ability to commercialize the HDF Assist Module, and other statements that are not historical facts, including statements that may be accompanied by the words “intends,” “may,” “will,” “plans,” “expects,” “anticipates,” “projects,” “predicts,” “estimates,” “aims,” “believes,” “hopes,” “potential” or similar words. Actual results could differ materially from those described in these forward-looking statements due to certain factors, including Nephros’ and SRP’s ability to achieve market acceptance of the HDF Assist Module, SRP’s lack of experience in commercializing technologies, the impact of the ongoing COVID-19 pandemic, uncertainty in clinical outcomes, changes in business, economic and competitive conditions, the availability of capital when needed, dependence on third-party manufacturers and researchers, regulatory reforms, uncertainties in litigation or investigative proceedings, and the availability of financing. These and other risks and uncertainties are detailed in Nephros’ reports filed with the U.S. Securities and Exchange Commission. Nephros does not undertake any responsibility to update the forward-looking statements in this release.
Investor Relations Contacts:
Kirin Smith, President
PCG Advisory, Inc.
(646) 823-8656
ksmith@pcgadvisory.com
Andy Astor, CEO
Nephros, Inc.
(201) 345-0824
andy.astor@nephros.com
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