" I Absolutely Love It." Gundry MD Bio Complete 3 Reaches Over 10 Million Units Sold
Gundry MD Bio Complete 3: A Breakthrough All-in-One Prebiotic, Probiotic, and Postbiotic Supplement to Support Gut Health, Digestion, and Energy
LOS ANGELES, May 1, 2025 /PRNewswire/ -- Gundry MD® is proud to announce that Bio Complete 3™, the company's flagship gut health supplement, has achieved a remarkable milestone: over 10 million units sold worldwide. This achievement underscores the growing recognition of Bio Complete 3's effectiveness in promoting optimal gut health.
Bio Complete 3 was meticulously crafted by Dr. Steven Gundry, a world-renowned heart surgeon and regenerative medicine practitioner. His dedication to advancing nutritional science led to the development of Bio Complete 3, a comprehensive solution designed to support digestive health and enhance overall vitality.
What is Gundry MD Bio Complete 3?
Gundry MD Bio Complete 3 is a cutting-edge, all-in-one dietary supplement designed to optimize gut health by combining the power of prebiotics, probiotics, and postbiotics. This advanced formula works to nourish beneficial gut bacteria, promote a balanced microbiome, and reinforce the gut lining, which is essential for proper digestion and nutrient absorption. By supporting a thriving gut environment, Bio Complete 3 helps reduce occasional bloating, gas, and irregular bowel movements, leading to improved digestive comfort.†*
In addition to enhancing digestion, Bio Complete 3 plays a key role in boosting energy levels by helping the body absorb essential nutrients more efficiently. The formula also helps curb cravings for unhealthy foods, making it easier to maintain a healthy diet and support weight management. A well-balanced gut microbiome has been linked to improved metabolic function, immune system support, and even enhanced cognitive health. By addressing gut health from multiple angles, Bio Complete 3 provides a comprehensive solution for those looking to improve their overall well-being from the inside out.
Gundry MD Bio Complete 3 Reviews
Key Ingredients in Gundry MD Bio Complete 3:
Gundry MD Bio Complete 3 FAQ
About Gundry MD
Founded in 2015, Gundry MD is dedicated to providing cutting-edge solutions to its users by using science-backed ingredients that can offer a boost in metabolism, sustained energy, smooth, easy digestion, and a youthful-feeling mind and body. These amazing results all begin with feeding your body powerful health-boosting nutrients like polyphenols. Based on his many years of nutrition research, Dr. Gundry helps create every Gundry MD product. Best-selling Gundry MD products include MCT Wellness, Total Restore, and Polyphenol-Rich Olive Oil. All Gundry MD products come with a 90-day purchase price guarantee (minus shipping) if you are not satisfied. For more information, visit www.gundrymd.com or @gundrymd on Instagram and Facebook.
About Dr. Gundry
Founder of Gundry MD, Dr. Steven Gundry was one of the world's top cardiothoracic surgeons Currently, he's the medical director at The International Heart and Lung Institute and The Centers for Restorative Medicine in Palm Springs and Santa Barbara, California where he's spent the past 25 years helping people restore their health by optimizing nutrition and lifestyle choices. Steven Gundry, MD is also the host of the top-ranked health podcast, The Dr. Gundry Podcast, and author of four New York Times best-selling books, including The Plant Paradox ™, which details his famous lectin-free diet. The Gut-Brain Paradox, Dr. Gundry's last book in April 2025, explores the fascinating breakthroughs between gut health and mental health. For more information, visit drgundry.com, the Dr. Gundry YouTube channel, Dr Gundry en Español, and follow @drstevengundry on Instagram and TikTok.
*All individuals are unique. Your results can and will vary.
Media Contact -
[email protected]
View original content to download multimedia: https://www.prnewswire.com/news-releases/-i-absolutely-love-it-gundry-md-bio-complete-3-reaches-over-10-million-units-sold-302443791.html
SOURCE Gundry MD
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles
Yahoo
2 hours ago
- Yahoo
Growth Hormone Deficiency Market to Register Incremental Growth at a CAGR of 5.7% During the Forecast Period (2025-2034)
The growth hormone deficiency market is expected to see expansion across the 7MM driven by the introduction of innovative therapies, including LUM-201 and SCO-240, among others. Furthermore, the rising prevalence of growth hormone deficiency, driven by improved diagnostics, higher survival rates of premature infants, increased pituitary disorders, and environmental factors like endocrine-disrupting chemicals, is expected to drive market growth for growth hormone replacement therapies. LAS VEGAS, June 10, 2025 /PRNewswire/ -- Growth hormone deficiency (GHD) is a rare condition resulting from inadequate secretion of growth hormone by the anterior pituitary gland. It can originate from birth, develop later in life, or have no known cause, underscoring the intricate mix of genetic, environmental, and diagnostic influences. Idiopathic cases are particularly difficult to address due to the absence of identifiable causes, revealing gaps in current understanding of the condition's underlying biology. According to DelveInsight, there were approximately 207,000 prevalent GHD cases across the 7MM in 2024, with around 165,000 diagnosed. This number is projected to increase by 2034. The United States accounted for the largest share of diagnosed prevalent cases in 2024, with roughly 70,000 cases—a figure expected to grow over the 2025–2034 forecast period. Current treatment options for GHD include approved therapies such as SOGROYA, SKYTROFA, and NGENLA. Standard treatment typically involves daily subcutaneous injections, which can be particularly burdensome for children, especially those with a fear of needles. Learn more about growth hormone deficiency treatment guidelines @ Growth Hormone Deficiency Treatment Market SOGROYA (somapacitan-beco) is a long-acting human growth hormone (hGH) analog that replicates the function of natural growth hormone. It's approved for children aged 2.5 years and older with growth failure due to insufficient endogenous GH and is also indicated as replacement therapy for adults with GHD. SOGROYA works by binding to a dimeric GH receptor on target cells, activating downstream signaling pathways, and producing effects largely mediated by liver-derived IGF-1. Key regulatory approvals include: FDA approval for adult GHD in August 2020 and for pediatric GHD in April 2023; EMA approval in March 2021; and PMDA approval in Japan for adult GHD in January 2021 and for pediatric growth issues in June 2023. SKYTROFA/TRANSCON hGH (lonapegsomatropin-tcgd) is a pegylated, long-acting hGH formulated for once-weekly subcutaneous administration. It's approved in both the US and EU for pediatric patients (aged ≥1 year, ≥11.5 kg) with growth failure due to inadequate GH levels. It binds to GH receptors, initiating intracellular signaling and delivering both direct (e.g., tissue and metabolic regulation) and indirect (via IGF-1) effects, including chondrocyte development, increased hepatic glucose production, protein synthesis, and fat breakdown. Regulatory milestones include FDA approval in August 2021 for pediatric GHD, EU approval in January 2022 for patients aged 3–18, and an sBLA accepted by the FDA in December 2024 for adult GHD, with a PDUFA decision expected in July 2025. NGENLA (somatrogon-ghla) is another long-acting hGH analog developed to address inadequate natural GH production. Approved for children aged 3 and above with growth failure, NGENLA distinguishes itself from daily-injection therapies like GENOTROPIN by offering once-weekly dosing through an adjustable delivery device. It binds GH receptors and activates STAT5b signaling, leading to elevated IGF-1 and promoting linear growth and metabolic effects. NGENLA is approved in the US, EU, and Japan for pediatric GHD and is undergoing global Phase III trials for adult GHD. Regulatory highlights include US FDA approval in June 2023, European Commission approval in February 2022, and PMDA approval in January 2022. In July 2024, OPKO Health entered into a USD 250 million non-dilutive note agreement with HealthCare Royalty, backed by profit-sharing proceeds from its 2014 global partnership with Pfizer. Find out more on FDA-approved growth hormone deficiency treatment @ Growth Hormone Deficiency Drugs Market Existing treatments for growth hormone deficiency typically involve subcutaneous injections, available in both daily and newer weekly formats. However, the need for daily administration can be particularly difficult for children, often resulting in low adherence. To address this issue and enhance patient compliance, researchers are developing long-acting and oral alternatives. Companies like Lumos Pharma and SCOHIA PHARMA are advancing their candidates through clinical trials, contributing to innovation in the growth hormone deficiency space and opening up substantial opportunities for market growth. Discover which therapies are expected to grab major growth hormone deficiency market share @ Growth Hormone Deficiency Therapy LUM-201 (ibutamoren), an oral small molecule developed by Lumos Pharma, functions as an agonist of the growth hormone secretagogue receptor to stimulate the natural pulsatile release of growth hormone (GH). This targeted approach supports its use in conditions requiring enhanced GH production. Clinical studies have shown that LUM-201 is both safe and consistently effective in promoting GH secretion. Notably, the Phase II OraGrowtH210 and OraGrowtH212 trials in children with pediatric growth hormone deficiency (PGHD) successfully met all primary and secondary endpoints, reinforcing the drug's therapeutic value. In 2017, LUM-201 was granted orphan drug designation (ODD) in both the US and EU for treating growth hormone deficiency, which provides development incentives. Data presented at the European Society for Paediatric Endocrinology conference in November 2024 demonstrated sustained growth over 24 months, affirming the effectiveness of its pulsatile secretion mechanism. In December 2024, Double Point Ventures acquired Lumos Pharma through a tender offer, paying USD 4.25 per share along with contingent value rights. SCO-240, from SCOHIA PHARMA, is an oral small molecule that selectively blocks Somatostatin Receptor 5 (SSTR5), a receptor involved in hormonal regulation. While the exact function of SSTR5 in humans remains under investigation, SCO-240 has shown encouraging results in enhancing GH secretion. In a Phase I clinical study, the drug triggered significant GH release without disrupting other pituitary hormones, underscoring the therapeutic potential of SSTR5 antagonism for GH-related conditions. The compound exhibited a strong safety profile, was well-tolerated, and is suitable for once-daily oral use. In June 2023, findings from the study were presented at the 96th Annual Congress of the Japan Endocrine Society, highlighting its promise in treating GH deficiency, female infertility, and alopecia. In February 2024, SCO-240 was selected for AMED's Orphan Drug Prior to Designation support program, securing funding for its continued development in PGHD. Discover more about drugs for growth hormone deficiency in development @ Growth Hormone Deficiency Clinical Trials The anticipated launch of these emerging therapies for growth hormone deficiency are poised to transform the market landscape in the coming years. As these cutting-edge therapies continue to mature and gain regulatory approval, they are expected to reshape the growth hormone deficiency market landscape, offering new standards of care and unlocking opportunities for medical innovation and economic growth. DelveInsight estimates that the market size for growth hormone deficiency is expected to grow from USD 1.4 billion in the 7MM in 2024 at a significant 5.7% CAGR by 2034. This growth across the 7MM is expected to be fueled by the launch of novel therapies such as LUM-201 and SCO-240, among others. Additionally, the increasing prevalence, attributed to advancements in diagnostic capabilities, improved survival rates of premature infants, a rise in pituitary disorders, and environmental influences like endocrine-disrupting chemicals, is projected to boost the demand for growth hormone replacement therapies. DelveInsight's latest published market report, titled as Growth Hormone Deficiency Market Insight, Epidemiology, and Market Forecast – 2034, will help you to discover which market leader is going to capture the largest market share. The report provides comprehensive insights into the growth hormone deficiency country-specific treatment guidelines, patient pool analysis, and epidemiology forecast to help understand the key opportunities and assess the market's underlying potential. The growth hormone deficiency market report proffers epidemiological analysis for the study period 2020–2034 in the 7MM, segmented into: Total Prevalent Cases of Growth Hormone Deficiency Total Diagnosed Prevalent Cases of Growth Hormone Deficiency Total Diagnosed Prevalent Cases of Pediatric Growth Hormone Deficiency Total Diagnosed Prevalent Cases of Adult Growth Hormone Deficiency Gender-specific Cases of Growth Hormone Deficiency Etiology-specific Cases of Growth Hormone Deficiency The report provides an edge while developing business strategies by understanding trends shaping and driving the 7MM growth hormone deficiency market. Highlights include: 10-year Forecast 7MM Analysis Epidemiology-based Market Forecasting Historical and Forecasted Market Analysis upto 2034 Emerging Drug Market Uptake Peak Sales Analysis Key Cross Competition Analysis Industry Expert's Opinion Access and Reimbursement Download this growth hormone deficiency market report to assess the epidemiology forecasts, understand the patient journeys, know KOLs' opinions about the upcoming treatment paradigms, and determine the factors contributing to the shift in the growth hormone deficiency market. Also, stay abreast of the mitigating factors to improve your market position in the growth hormone deficiency therapeutic space. Related Reports Growth Hormone Deficiency Epidemiology Forecast Growth Hormone Deficiency Epidemiology Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted GHD epidemiology in the 7MM, i.e., the United States, EU4 (Germany, Spain, Italy, France) and the United Kingdom, and Japan. Growth Hormone Deficiency Pipeline Growth Hormone Deficiency Pipeline Insight – 2025 report provides comprehensive insights about the pipeline landscape, pipeline drug profiles, including clinical and non-clinical stage products, and the key GHD companies, including Novo Nordisk, Ascendis Pharma, among others. Adult Growth Hormone Deficiency Market Adult Growth Hormone Deficiency Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key adult growth hormone deficiency companies, including Novo Nordisk, Ascendis Pharma, among others. Pediatric Growth Hormone Deficiency Market Pediatric Growth Hormone Deficiency Market Insights, Epidemiology, and Market Forecast – 2034 report delivers an in-depth understanding of the disease, historical and forecasted epidemiology, as well as the market trends, market drivers, market barriers, and key pediatric growth hormone deficiency companies, including TJ Biopharma, Lumos Pharma, SCOHIA PHARMA, Inc., among others. About DelveInsight DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports pharma companies by providing comprehensive end-to-end solutions to improve their performance. Get hassle-free access to all the healthcare and pharma market research reports through our subscription-based platform PharmDelve. Contact Us Shruti Thakur info@ +14699457679 Logo: View original content: SOURCE DelveInsight Business Research, LLP Melden Sie sich an, um Ihr Portfolio aufzurufen.
Yahoo
2 hours ago
- Yahoo
NanoHive Medical Sublicenses DirectSync's Piezoelectric Patents to Explore Development of Hive™ Soft Titanium® 3D Printed Spine Interbody Fusion "Smart Implant"
BOSTON, June 10, 2025 /PRNewswire/ -- NanoHive Medical, LLC, a leading innovative 3D printed spinal implant technology company is pleased to announce that the company has secured the exclusive sublicense of DirectSync Surgical's piezoelectric implantable sensor technology for the field of spinal fusion. DirectSync Surgical had licensed the technology from the University of Kansas. NanoHive is exploring the advancement of successful proof-of-concept research to potentially develop bone stimulating and remote monitoring/data collection sensor technology housed in the company's highly innovative spinal interbody fusion device lattice which is currently commercialized in the company's Hive™ Soft Titanium® portfolio of 3D printed spinal interbody fusion devices. In October 2023, the company reported the initiation of a research collaboration with DirectSync Surgical. Based on the preliminary research generated, the company ascertained that their proprietary rhombic dodecahedron lattice technology was uniquely capable of transferring significant energy from the encapsulated piezoelectric sensor. The company is currently in the process of working with the US Food and Drug Administration (FDA) on the transfer of the Breakthrough Device Designation from DirectSync to NanoHive. Patrick O'Donnell, President & CEO of NanoHive stated, "NanoHive's Soft Titanium® technology is the ideal interbody fusion implant to deliver a sensor with data collection and bone stimulation capability. The company is excited about the prospect of leading the way with the development of a technological leap in the interbody fusion device category. Our view of the future of innovation in spine devices emphasizes that new technologies must demonstrate an improvement to patient virtual care and clinical outcomes as well as connectivity with enabling surgical technologies and artificial intelligence. These advancements must also deliver cost-efficiencies to the various stakeholders involved in the spine patient's episode-of-care. More meaningful and frequent data collection that can ultimately be utilized as a predictive tool will be essential to this vision." About NanoHive Medical LLC NanoHive Medical is a pioneer and leading innovator in 3D printed spinal interbody fusion implants and instrumentation. The company's proprietary, biomimetic Soft Titanium® technology clearly distinguishes their products in the $2.4B U.S. spinal interbody fusion device market. The Hive™ portfolio of interbody fusion devices provide surgeons and their patients ideal biomechanical elastic modulus properties, clear and precise diagnostic imaging capability, osteoblast cell attraction and integration – all features that lead to consistently strong fusion constructs and efficacious clinical experiences. NanoHive Medical is based in Woburn, Massachusetts U.S.A. Contact: Patrick O'Donnell, CEO & President, NanoHive Medical LLC, Website: About DirectSync Surgical DirectSync Surgical is a rising leader in smart patient powered implant devices. With a commitment to innovation and foundational research, the company develops and manufactures advanced tools that empower both spinal and orthopedic professionals to achieve superior surgical outcomes. DirectSync Surgical's products are not available for sale in the US. Contact: Leighton LaPierre, COO, DirectSync Surgical, leighton@ Website: NanoHive Medical, LLC | 12 Gill Street, Suite 4500 | Woburn, MA 01801 | 844-943-5433 View original content to download multimedia: SOURCE NanoHive Medical Error in retrieving data Sign in to access your portfolio Error in retrieving data Error in retrieving data Error in retrieving data Error in retrieving data
Yahoo
2 hours ago
- Yahoo
Applied Medical Technology, Inc. Unveils Redesigned Mobile App Aligned with Recent Website Refresh
BRECKSVILLE, Ohio., June 10, 2025 /PRNewswire/ -- Applied Medical Technology, Inc. (AMT), a leader in innovative medical devices, is proud to announce the launch of its redesigned mobile application, AMT ONE Source®. This strategic update follows a successful website redesign completed late 2024, ensuring that both platforms now offer a cohesive, user-friendly digital experience. Enhancing User Experience Across PlatformsThe redesigned mobile app mirrors the modern, intuitive design language introduced during the website refresh. With a renewed focus on user experience and engagement, the mobile platform now features streamlined interfaces and updated information. "In today's fast-paced healthcare environment, it is essential that our digital platforms are not only reliable but also easy to navigate and visually appealing," said Bill Bentley, National Sales Manager. "Created with our youngest patients in mind, the redesign was thoughtfully developed to be more engaging, age-appropriate, and easy to navigate—helping children and their families feel more supported and empowered throughout their healthcare journey." Key Features and Benefits Unified Design Aesthetic: The mobile app adopts the clean, modern design previously launched on the website, providing a consistent look and feel across all digital touchpoints. Richer Content Experience: The app now features an expanded content database, providing a broader range of resources and information to support users with timely, relevant, and easy-to-access content. Improved Performance: The redesigned app features enhanced performance, with a new backend architecture that allows for faster content updates, easier maintenance, and more frequent improvements to keep the experience fresh and relevant. AMT partnered with Cleveland-Ohio based software company, Stream 9, on the redesign. Their strong track record in software design and development brought deep technical expertise and a strategic approach. "We're fortunate in our business to develop custom software projects for businesses of all kinds; but it's especially rewarding to work on a project that will deliver such a direct benefit to patients and their caregivers. AMT brought a clear vision to the table, and we worked closely together to translate that into a modern, scalable, and user-friendly digital experience," shared Kirk Miesle, Founder of Stream 9. The AMT ONE Source® app is available now on the App Store and Google Play. About AMT: Applied Medical Technology, Inc. (AMT) is a global leader in enteral and surgical devices committed to improving lives through innovation. For 40 years, AMT has bridged the gap between medical technology and patient needs, collaborating with healthcare professionals and users to develop high-quality, life-enhancing solutions. Our holistic approach prioritizes the well-being of the whole person, not just the device they use. View original content to download multimedia: SOURCE Applied Medical Technology, Inc.