Patient Monitoring & Vital Signs in Nevada

Entegrion, Inc. is a life sciences company specializing in viscoelastic coagulation monitoring (VCM) systems for rapid hemostasis assessment. The company develops point-of-care diagnostic instruments designed to measure blood coagulation in real-time, enabling clinicians to manage hemostasis and coagulopathies across trauma, surgery, obstetrics, and emergency medicine settings. The VCM system uses fully automated testing with fresh whole blood—no chemical accelerants or sample manipulation required—making it suitable for bedside and pre-hospital applications. The device features a portable footprint optimized for multiple clinical environments. Entegrion's products address both civilian and military medicine needs; the U.S. Department of Defense has invested over $100 million in the company's product development since inception. The VCM has achieved CE Mark regulatory clearance in Europe and other regions accepting CE-marked devices; however, it has not yet received FDA 510(k) clearance for human clinical use in the United States. The company also offers VCMVet for veterinary coagulation monitoring and VCM Cascade for human applications. Leadership includes experienced healthcare executives and clinicians with backgrounds in emergency medicine, hematology, laboratory diagnostics, and transfusion medicine. The organization combines R&D, clinical validation, and regulatory expertise to bring complex laboratory tests to point-of-care settings.

Perimed AB is a Swedish medical device manufacturer specializing in noninvasive vascular diagnostics and microcirculation assessment. Founded in the early 1980s, the company leverages laser Doppler flowmetry and laser speckle contrast imaging (LSCI) technologies to measure blood perfusion, microcirculation, and oxygen delivery in clinical and research settings. The company offers two primary product lines: PeriFlux systems for comprehensive vascular assessment (measuring toe pressure, segmental limb pressure, transcutaneous oxygen pressure, and skin perfusion pressure) and PeriCam systems for real-time perfusion imaging. Key instruments include the PeriFlux 6000 Combined System, PeriFlux 6000 EPOS (Enhanced Perfusion and Oxygen Saturation), and PeriCam PSI NR (on mobile cart for clinical and surgical use). Applications span diabetic foot complications, peripheral artery disease (PAD), wound healing assessment, hyperbaric oxygen therapy monitoring, dermatology, and preclinical research including cerebral blood flow monitoring, angiogenesis, hindlimb ischemia, and tumor models. The company maintains a US office in Las Vegas, Nevada, and headquarters in Järfälla, Sweden. Products are designed for clinical diagnosis, treatment planning, research protocols, and long-term therapeutic monitoring. The technology enables noninvasive, contact-free measurement with real-time visualization and comprehensive reporting capabilities.

Fudakang Industrial Co Ltd is a medical device manufacturer specializing in homecare monitoring equipment and personal health devices. The company produces a range of blood pressure monitors, thermometers (infrared and digital), and related consumables designed for home use and daily patient monitoring. Their product portfolio includes multiple models of automated blood pressure monitors with varying cuff sizes (standard through XXL), digital thermometers with multiple display options, accessories such as probe covers and replacement cuffs, and AC-DC power adapters. Products feature multilingual interfaces supporting English and Spanish, addressing diverse patient populations. The company serves seniors and individuals requiring ongoing in-home health monitoring. Fudakang markets its devices through a direct B2B and B2C distribution model, offering product catalogs and dealer/partnership programs. The company appears to maintain regulatory compliance with UL certifications on power adapters. Product lines are identified by model codes (e.g., FT-B22Y, FT-C02-V, BT-A21CN, 3R-480140-01), suggesting established manufacturing and quality control processes. The website indicates warranty registration capabilities and customer support infrastructure. While specific FDA 510(k) or ISO 13485 certifications are not explicitly mentioned on the homepage, the product quality and design suggest compliance with medical device regulations for home monitoring equipment.