Legacy MEDSearch

AUGUST 8, 2022

MicroPort Navibot has received 510(K) clearance from the Food and Drug Administration (FDA) in the United States for the SkyWalker System, the company’s first robot-assisted platform for orthopedic applications. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry.

Food and Drug Administration 98

Food and Drug Administration Recruitment Medical Management 98

Legacy MEDSearch

SEPTEMBER 27, 2022

Food and Drug Administration (FDA) 510(k) clearance for its CellFX System, expanding the indication for use to include the treatment of sebaceous hyperplasia in patients with Fitzpatrick skin types I-III. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry.

FDA 98

FDA Food and Drug Administration Recruitment Medicine 98

Legacy MEDSearch

DECEMBER 12, 2022

IRRAS markets and sells its comprehensive, innovative IRRAflow and Hummingbird ICP Monitoring product lines to hospitals worldwide through its direct sales organization in the United States and select European countries as well as an international network of distribution partners. For more information, please visit www.irras.com.

FDA 95

FDA Food and Drug Administration Recruitment Medical 95

Legacy MEDSearch

SEPTEMBER 16, 2022

Food and Drug Administration (FDA) has cleared its Tasso+ lancet as a Class II medical device. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Tasso, Inc., the leading provider of convenient, clinical-grade blood collection solutions, announced that the U.S.

Medical 97

Medical FDA Food and Drug Administration Recruitment 97

Legacy MEDSearch

JANUARY 19, 2023

Food and Drug Administration (FDA) 510(k) clearance for the Flex-Thread Ulna Intramedullary (IM) Nail System. Conventus Flower Orthopedics, an innovation-driven medical technology company, announced they have received U.S. Our clients include both blue-chip companies and innovative startups within the MedTech space.

Food and Drug Administration 97

Food and Drug Administration FDA Recruitment Marketing 97

Legacy MEDSearch

DECEMBER 6, 2022

Activ Surgical received 501(k)-clearance for ActivSight by the Food and Drug Administration (FDA) in the United States in 2021. To date, multiple major hospital networks across the U.S. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry.

Food and Drug Administration 98

Food and Drug Administration Safety Recruitment Medical 98

Legacy MEDSearch

JANUARY 4, 2023

Food and Drug Administration (FDA) 510(k) clearance of the BiWaze ® Clear System. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. We pride ourselves on our professionalism and ability to communicate quickly and honestly with all parties in the hiring process.

FDA 95

FDA Food and Drug Administration Recruitment Management 95

Legacy MEDSearch

JUNE 7, 2022

Food and Drug Administration (FDA) clearance for the company’s FreedomFlow® Peripheral Guidewire. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. appeared first on Legacy MedSearch | Medical Device Recruiters. Cardio Flow, Inc., The post Cardio Flow, Inc.,

Food and Drug Administration 98

Food and Drug Administration FDA Recruitment Medical 98

Legacy MEDSearch

FEBRUARY 21, 2023

Food and Drug Administration (FDA) 510(k) clearance for DiLumen EZ¹, a single-use, disposable endotherapy device for endoscopic mucosal resections (EMR) and difficult colonoscopies. The post Lumendi Receives 510(k) Clearance for Two New Devices appeared first on Legacy MedSearch | Medical Device Recruiters.

Food and Drug Administration 98

Food and Drug Administration Recruitment Medical Distribution 98

Legacy MEDSearch

JANUARY 31, 2023

Food and Drug Administration has approved the company’s fourth-generation rechargeable sacral neuromodulation system. The post Axonics Receives FDA Approval for Fourth-Generation Rechargeable Sacral Neuromodulation System appeared first on Legacy MedSearch | Medical Device Recruiters. Axonics, Inc.,

FDA 98

FDA Food and Drug Administration Recruitment Medical 98

Legacy MEDSearch

DECEMBER 8, 2022

Food and Drug Administration (FDA). Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. The post Promising Remote Patient Monitoring solution, Polso, Achieves 1st FDA Clearance appeared first on Legacy MedSearch | Medical Device Recruiters.

FDA 97

FDA Patients Food and Drug Administration Medical 97

Legacy MEDSearch

DECEMBER 21, 2022

Food and Drug Administration (FDA) for 510(k) clearance. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. We pride ourselves on our professionalism and ability to communicate quickly and honestly with all parties in the hiring process.

Manufacturing 98

Manufacturing FDA Food and Drug Administration Medical 98

Legacy MEDSearch

JANUARY 10, 2023

Food and Drug Administration (FDA). Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. The post VERO Biotech Receives FDA Approval of its Third Generation Tankless Inhaled Nitric Oxide Delivery System appeared first on Legacy MedSearch | Medical Device Recruiters.

FDA 98

FDA Food and Drug Administration Recruitment Management 98

Legacy MEDSearch

NOVEMBER 15, 2022

Food and Drug Administration (FDA) 510(k) clearance for its new NiTy+ One-Shot Staple Fixation System. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Our clients include both blue-chip companies and innovative startups within the MedTech space.

Medical 98

Medical FDA Food and Drug Administration Engineering 98

Legacy MEDSearch

NOVEMBER 28, 2022

Food and Drug Administration for commercial use in the United States. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. The post NeuroLogica Announces FDA 510(k) Clearance of BodyTom® 64 appeared first on Legacy MedSearch | Medical Device Recruiters.

FDA 92

FDA Food and Drug Administration Electronics Recruitment 92

Legacy MEDSearch

SEPTEMBER 12, 2022

Food and Drug Administration (FDA) 510(k) clearance and launch of a next-generation RhinAer® stylus. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Aerin Medical Inc., Our clients include both blue-chip companies and innovative startups within the MedTech space.

Medical 98

Medical Patients FDA Physicians 98

Legacy MEDSearch

NOVEMBER 9, 2022

Food and Drug Administration. Over the past 17 years, we have built one of the strongest networks of device professionals ranging from sales, marketing, research & , quality & regulatory, project management, field service, and clinical affairs. Saranas, Inc.

Patients 98

Patients Food and Drug Administration Physicians Recruitment 98

Legacy MEDSearch

MARCH 13, 2023

Food and Drug Administration (FDA) has granted an Investigational Device Exemption (IDE) to advance the company’s PATCH Clinical Study, a multi-center, single-arm, pivotal study evaluating the safety and effectiveness of the Vivasure PerQseal ® Closure Device System.

Medical 98

Medical FDA Food and Drug Administration Recruitment 98

Legacy MEDSearch

MARCH 15, 2023

HeartBeam AIMI and HeartBeam AIMIGo have not yet been cleared by the US Food and Drug Administration (FDA) for marketing in the USA or other geographies. The post HeartBeam Announces Acquisition of LIVMOR Assets appeared first on Legacy MedSearch | Medical Device Recruiters. For more information, visit HeartBeam.com.

Food and Drug Administration 97

Food and Drug Administration FDA Recruitment Physicians 97

Legacy MEDSearch

JANUARY 12, 2023

Food and Drug Administration (FDA) has granted the coveted Breakthrough Device Designation for its LifeGel Absorbable Surgical Hemostat. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Medcura, Inc.,

Food and Drug Administration 97

Food and Drug Administration FDA Recruitment Medical 97

Legacy MEDSearch

JUNE 17, 2022

Food and Drug Administration (FDA) 510(k) clearance of the LOBO-7 and LOBO-9 Vascular Occluders, the latest addition to the company’s LOBO ® Vascular Occlusion System. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Okami Medical Inc.,

Medical 90

Medical FDA Food and Drug Administration Recruitment 90

Legacy MEDSearch

DECEMBER 1, 2022

Food and Drug Administration (FDA) for the Quantra Hemostasis System with QStat Cartridge. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Our clients include both blue-chip companies and innovative startups within the MedTech space.

FDA 95

FDA Food and Drug Administration Recruitment Medical 95

PM360

FEBRUARY 12, 2024

Given that less than 10% of rare diseases currently have an available treatment approved by the United States Food and Drug Administration (FDA) , advocating for the speedy development of novel drugs and therapies is a crucial step in improving the quality of life for those affected. What is a Rare Disease?

Food and Drug Administration 105

Food and Drug Administration Patients Medical Networking 105

Legacy MEDSearch

MARCH 7, 2024

Food and Drug Administration (FDA) announced the clearance of Dexcom’s device, marking it as the first continuous glucose monitor available over the counter. On March 5, the U.S. Following this announcement, Dexcom’s shares experienced a 2.2% increase in extended trading.

Food and Drug Administration 52

Food and Drug Administration FDA Food Management 52

Legacy MEDSearch

MARCH 1, 2024

Boston Scientific’s AGENT Drug-Coated Balloon (DCB) has been granted approval by the U.S. Food and Drug Administration (FDA) for treating coronary in-stent restenosis (ISR) in patients with coronary artery disease. Our clients include both blue-chip companies and innovative startups within the MedTech space.

Food and Drug Administration 52

Food and Drug Administration FDA Recruitment Physicians 52

Legacy MEDSearch

OCTOBER 30, 2023

Medinol today announced United States Food and Drug Administration (FDA) approval for the EluNIR-PERL drug-eluting stent (DES) for the treatment of coronary artery disease. EluNIR-PERL builds upon the proven performance and clinical data of the EluNIR DES system. “We are pleased to bring technologies to the U.S.

Food and Drug Administration 52

Food and Drug Administration FDA Distribution Recruitment 52

Legacy MEDSearch

MARCH 1, 2023

a medical imaging company focused on improving the treatment and outcomes for patients with coronary artery disease (CAD), today announced Food and Drug Administration (FDA) 510(k) clearance of their flagship intravascular imaging system, HyperVue. SpectraWAVE, Inc.,

Food and Drug Administration 97

Food and Drug Administration Physicians Recruitment Medical 97

Legacy MEDSearch

NOVEMBER 14, 2022

Food and Drug Administration (FDA). Food and Drug Administration cleared the software for use in 2022. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Xironetic is headquartered in Oklahoma City.

Food and Drug Administration 52

Food and Drug Administration FDA Recruitment Food 52

Legacy MEDSearch

JANUARY 18, 2023

Food and Drug Administration (FDA) 510(k) clearance to aid in the early detection of sepsis for the approximately 30 million adult patients with signs and symptoms of infection who present to US emergency departments (ED) each year. For updates, follow Cytovale on LinkedIn and Twitter.

Food and Drug Administration 98

Food and Drug Administration FDA Recruitment Medical 98

Legacy MEDSearch

MARCH 27, 2023

Food and Drug Administration (FDA) 510(k) clearance for its FalloView device. Food and Drug Administration (FDA) 510(k) clearance for its FalloView device. Receives FDA Clearance For Its FalloView™ Falloposcope appeared first on Legacy MedSearch | Medical Device Recruiters. FemDx Medsystems, Inc.,

Food and Drug Administration 52

Food and Drug Administration FDA Recruitment Physicians 52

Legacy MEDSearch

APRIL 11, 2023

Food and Drug Administration (FDA) granted marketing authorization of the MISHA Knee System, an implantable shock absorber (ISA) for the knee. The post FDA Authorizes Marketing of MISHA™ Knee System for People Suffering from Knee Osteoarthritis appeared first on Legacy MedSearch | Medical Device Recruiters.

Marketing 96

Marketing FDA Food and Drug Administration Recruitment 96

Pharmaceutical Technology

JUNE 15, 2023

The need for new medical treatments and drugs has never been greater. But before pharmaceutical companies can go to market with a breakthrough drug, they need to ensure safety and efficacy through clinical trials. Even reaching the clinical trial phase offers no guarantees, as only 12% of such drugs receive U.S.

Food and Drug Administration 52

Food and Drug Administration Side effects Recruitment Safety 52

Legacy MEDSearch

OCTOBER 24, 2023

Food and Drug Administration (FDA) for its novel coronary artery bifurcation stenting technology. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Receives FDA Breakthrough Device Designation appeared first on Legacy MedSearch | Medical Device Recruiters.

FDA 52

FDA Food and Drug Administration Recruitment Food 52

Legacy MEDSearch

FEBRUARY 3, 2023

Food and Drug Administration (FDA) has granted the first marketing clearance for its SCINTIX biology-guided radiotherapy, a cutting-edge treatment applicable for early and late-stage cancers. RefleXion Medical , a therapeutic oncology company, announced the U.S.

FDA 97

FDA Food and Drug Administration Medical Recruitment 97

Legacy MEDSearch

MARCH 21, 2023

a privately held company focused on innovative fluorescence-guided imaging technologies for cancer surgery, today announced a New Drug Application (NDA) for its LUMISIGHT Optical Imaging Agent has been submitted to the U.S. Food and Drug Administration (FDA). Lumicell, Inc.,

Food and Drug Administration 52

Food and Drug Administration FDA Recruitment Medical 52

Legacy MEDSearch

MAY 24, 2022

Food and Drug Administration (FDA) 510(k) clearance for DiLumen EZ¹, a single-use, disposable endotherapy device intended for endoscopic mucosal resections (EMR) and difficult colonoscopies. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry.

Food and Drug Administration 52

Food and Drug Administration FDA Recruitment Food 52

Legacy MEDSearch

DECEMBER 20, 2022

Food & Drug Administration (FDA) submission process for the LimiFlex Dynamic Sagittal Tether (DST). Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Empirical Spine, Inc.,

FDA 94

FDA Food and Drug Administration Recruitment Patients 94