Business Wire

FL-UVLRX-THERAPEUTICS

31.3.2016 08:04:23 CEST | Business Wire | Press release

Share
Intravenous Light Therapy Demonstrates Huge Potential for Aesthetic Medicine

In anticipation of its official European launch at the 14th Aesthetic & Anti-Aging Medicine World Congress (AMWC) this month, UVLrx Therapeutics™ is pleased to share its intravenous light therapy treatment system, the model UVL1500, to assist in aesthetic post-surgical and non-surgical patient recovery by reducing inflammation, pain, and accelerating wound repair. The company has started to collect patient data that showcases the benefits of light wavelengths utilized by its UVLrx™ Treatment System* for reducing inflammation, a key issue following invasive and non-invasive aesthetic procedures today.

This Smart News Release features multimedia. View the full release here: http://www.businesswire.com/news/home/20160330006331/en/

“According to the International Society of Aesthetic Plastic Surgery , more than 20 million cosmetic surgical and non-surgical procedures were performed in 2014,” said Michael Harter, CEO and president of UVLrx. “The success of those procedures depends heavily on quality of recovery and patient response, which is why inflammation abatement is so important for the industry. By immediately reducing inflammation caused by an aesthetic procedure, our technology may minimize pain and accelerate healing, which in turn may lead to better results and a more satisfied post-op patient.”

Dr. Daniel Knight, MD, and Denise Moss, RN, in conjunction with White Clover Wellness & Research Center in Shreveport, Louisiana, have clinical trial results that demonstrate recovery improvement using an investigational device version of the UVLrx technology (Model UVL1000) by reducing pain, edema and erythema in several of their post-surgical/non-surgical aesthetics patients. In fact, all fifteen patients they treated recently in the clinical trial reported improvement in overall quality of life and confidence in their recovery progression. The patients’ positive perception of their improved recovery even appeared to translate into the patients’ perception of how successful the results of their aesthetic procedures were overall, in some cases even accelerating results.

In this clinical trial, patients were treated and subsequently monitored across four evaluation points: baseline and days 3, 7 and 14 post-procedure. Subjects reported improvement by day 3 evaluation, and no adverse effects have been observed. UVLrx patients reported a significant reduction in pain and presented with impressive clinical results days after undergoing non-surgical procedures such as transdermal ultrasound skin tightening, which has often been described as painful and requiring several months to observe clinical results. The level of post-procedural progress observed in this study by day 7 resembled results typically observed in months 2 and 3 post procedure.

“Aesthetic physicians’ work is judged not only by procedural results but also by their patients’ recovery experiences,” commented Rowland Hanson, chairman of UVLrx. “Given the recent Centers for Disease Control and Prevention (CDC) guidelines regarding opiates in the U.S., we expect physicians to seek alternative pain management therapies such as the UVLrx™ Treatment System in order to avoid prescribing addictive and potentially fatal painkillers. Because many aggressive aesthetic procedures have required powerful opiates in the past, intravenous light therapy has the potential to mitigate this crisis and help aesthetics patients who suffer from post-procedural pain.”

Ultraviolet Blood Irradiation (UBI) has been used for over a century to treat bacterial and viral infections and was awarded a Nobel Prize for treating lupus in 1903. Routinely used in hospitals around the world, this form of light therapy fell out of prominence in the U.S. with the advent of antibiotics in the 1950s. With the recent expansion of drug-resistant infections, blood irradiation offers significant advantages to pharmaceutical therapies. Furthermore, UVLrx’s intravenous system is superior to existing ultraviolet blood irradiation (UBI) in that it does not require removal of blood from the body.

To learn more, visit UVLrx.com and stop by the UVLrx Therapeutics booth (F18) at the 14th Aesthetic & Anti-Aging Medicine World Congress from March 31st to April 2nd . To watch a webinar about UVLrx’s technology, please visit https://youtu.be/_WxFjQIekzM .

The UVLrx Station™ Model UVL1500 is not available for sale in the U.S.

* References to published specific wavelength studies available upon request.

About UVLrx Therapeutics

Based in Oldsmar, Florida, UVLrx Therapeutics is dedicated to evidence-based medicine in the field of light therapy and offers the first intravenous, concurrent delivery of ultraviolet-A (UVA) and multiple visible light wavelengths for treating a variety of medical indications. In addition to two Nobel Prizes and NASA-backed research, hundreds of international clinical trials have verified the health benefits of UV and other wavelengths of light utilized in the UVLrx™ Treatment System. For more information, please visit http://uvlrx.com .

Contact:

Press Contact:
Crier Communications
JP Lincoln
President
310-274-1072 x 201
jp@crierpr.com
or
Business Contact:
UVLrx Therapeutics
Rowland Hanson
Chairman
Rowland@UVLrx.com

Link:

ClickThru

About Business Wire

Business Wire
Business Wire
101 California Street, 20th Floor
CA 94111 San Francisco

http://businesswire.com

Subscribe to releases from Business Wire

Subscribe to all the latest releases from Business Wire by registering your e-mail address below. You can unsubscribe at any time.

Latest releases from Business Wire

Smartstream Smart Agents Delivers 70% Reduction in Back-Office Investigation Time, Proving the Case for Autonomous Operations26.3.2026 10:30:00 CET | Press release

Smartstream, the trusted data solutions provider for leading global financial institutions and enterprises, today announces that Smart Agents - its agentic AI solution for bank back-office operations is delivering measurable, transformational impact, with pilot results showing a 70% reduction in investigation time per user, per break. As the industry accelerates toward a service as software (SaS) operating model, and allowing more work to get done from software solutions, Smartstream is embracing this approach with agentic AI. The results validate a fundamental shift in how financial institutions approach exception management. In one benchmark scenario, the manual processing of 500 exceptions, typically requiring 116 hours of team effort, was reduced to just a few hours under fully autonomous operations. This eliminates swivel-chair workflows and frees up teams to focus on risk oversight, decision making, and higher-value activities. Institutions continue to struggle with back-office w

Infobip Supports Thousands of Startups and Scaleups Through Startup Tribe Programme26.3.2026 10:00:00 CET | Press release

In the first five years of the programme, Infobip has provided significant value in products and services to members, helping them build and scale customer communications worldwide Global AI-first cloud communications platform Infobip, which is celebrating its 20th anniversary this year, has supported thousands of startups and scaleups from over 120 countries in the first five years of its Startup Tribe Programme. Infobip launched its Startup Tribe Programme in May 2021 to help mission-driven startups and scaleups to build and manage their customer communications and engagement strategy and grow their business. It does this by providing access up to $60,000 in credits for Infobip’s services and its global network of advisors, investors, and accelerators. In the first five year, Infobip has provided millions in the value of products and services to its programme members. By eliminating the need to build a global communications infrastructure from the ground up, Infobip’s programme enabl

LTM Positioned as a Leader in ISG’s Provider Lens™ Evaluation for Oracle Cloud and Technology Ecosystem 202526.3.2026 09:58:00 CET | Press release

Recognition highlights LTM’s leadership across key quadrants in the United States and Europe LTM, the Business Creativity partner to the world’s largest enterprises, has been recognized as a Leader in multiple quadrants in the ISG Provider Lens™ Oracle Cloud and Technology Ecosystem 2025 reports for both the United States and Europe by Information Services Group (ISG), a leading global technology research and advisory firm. The ISG Provider Lens™ study evaluates leading Oracle ecosystem service providers across critical capability areas, including: Professional Services Managed Services OCI Solutions and Capabilities LTM’s positioning as a Leader across key quadrants in both regions reflects its strong Oracle ecosystem expertise, AI-led transformation approach, and proven track record in delivering large-scale enterprise cloud modernization programs. In its 2025 study, ISG highlights that the Oracle ecosystem is undergoing a fundamental shift toward AI-native architectures, multicloud-

Bureau Veritas Strengthens Global Sustainable Finance Capabilities with Expanded Climate Bonds Approved Verifier Status26.3.2026 08:30:00 CET | Press release

Bureau Veritas, a global leader in Testing, Inspection, and Certification services (TIC), is pleased to announce the expansion of its geographical scope as an Approved Verifier under the Climate Bonds Standard and Certification Scheme. Additional offices in China, Japan, India, and France are now formally listed in the Climate Bonds Verifiers Directory. This expansion builds on Bureau Veritas’ established role since the approval of its Brazilian office in 2020, further enhancing its ability to support issuers with high-quality, independent verification services across key markets. “Our expanded presence as an Approved Verifier under the Climate Bonds Standard reinforces Bureau Veritas’ commitment to advancing credible, high‑integrity sustainable finance”, said Marc Roussel, Executive Vice President, Urbanization and Assurance at Bureau Veritas. “With verifier capabilities available across key markets, we continue to deliver local expertise with global assurance standards; boosting mark

Invivoscribe® Expands IVDR Portfolio with IdentiClone® Dx IGH Assay Certification26.3.2026 06:13:00 CET | Press release

IdentiClone® Dx IGH is the first IVDR-certified assay for the detection of clonal immunoglobulin gene rearrangements in patients with suspected B-cell lymphoproliferative disease. Invivoscribe, a global leader in precision diagnostics and measurable residual disease (MRD) testing, is proud to announce that its IdentiClone Dx IGH Assay has received In Vitro Diagnostic Regulation (IVDR) 2017/746 Class C certification in the European Union (EU). Commercial availability of the IVDR-certified assay is anticipated by early April 2026. The IVDR replaces the former In Vitro Diagnostics Directive (IVDD), introducing significantly more stringent requirements for clinical evidence, performance evaluation, traceability, and post-market surveillance. Under IVDR, in vitro diagnostic devices are classified according to risk from Class A (lowest risk) to Class D (highest risk). Class C devices, such as IdentiClone Dx IGH, are considered high-risk tests that play a critical role in disease diagnosis an

In our pressroom you can read all our latest releases, find our press contacts, images, documents and other relevant information about us.

Visit our pressroom
World GlobeA line styled icon from Orion Icon Library.HiddenA line styled icon from Orion Icon Library.Eye