Legacy MEDSearch

OCTOBER 18, 2023

Food and Drug Administration (FDA) 510(k) clearance for the company’s FreedomFlow Orbital Atherectomy Peripheral Platform. Food and Drug Administration (FDA) 510(k) Clearance for its FreedomFlow® Orbital Atherectomy Peripheral Platform Press Release by: Cardio Flow, Inc. Cardio Flow, Inc. , Announces U.S.

Food and Drug Administration 52

Food and Drug Administration Food FDA Physicians 52

Legacy MEDSearch

OCTOBER 25, 2022

EndoStim , a medical device company developing and commercializing a first-in-class implantable neurostimulation treatment for drug refractory gastroesophageal reflux disease (GERD), announced that the U.S. Food and Drug Administration (FDA) granted Breakthrough Device Designation for the Company’s EndoStim System.

Food and Drug Administration 98

Food and Drug Administration FDA Recruitment Side effects 98

World of DTC Marketing

APRIL 7, 2021

I have to laugh when I hear that a pharma company is patient-centric because that’s become a slogan to make employees feel good about themselves while the costs of prescription drugs increase every year. drug spending by 9 percent” What about taxpayers? Highest-paid CEOs in 2019: Who made the list from healthcare.

Healthcare 162

Healthcare Healthcare Food and Drug Administration Pharma 162

European Pharmaceutical Review

NOVEMBER 9, 2023

Following her presentation on age-related disease at BioFuture 2023, Executive Vice President of Drug Development for MyMD Pharmaceuticals ® , Jenna Brager, shares with EPR why the company’s next-generation tumour necrosis factor (TNF)-alpha inhibitor has potential in inflammatory and autoimmune disorders.

Food and Drug Administration 115

Food and Drug Administration Side effects Pharmaceutical Leads 115

World of DTC Marketing

FEBRUARY 4, 2021

Merck’s old drugs are under more scrutiny, and anti-vaxxers are causing problems by cherry-picking unreliable information. I am reminded of a business colleague who left a company in the midwest after being recruited heavily by Amgen. prescriptions of finasteride, as the drug is known, for hair loss increased to over 2.4

Pharma 180

Pharma Food and Drug Administration Side effects Safety 180

Legacy MEDSearch

NOVEMBER 1, 2022

Food & Drug Administration (FDA) for its smaller-diameter CurvaFix® IM Implant indicated for fixation of fractures of the pelvis. Food & Drug Administration (FDA). Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. CurvaFix, Inc.,

Food and Drug Administration 98

Food and Drug Administration FDA Recruitment Food 98

Pharmaceutical Technology

AUGUST 12, 2022

In June this year, it was announced that the US Food and Drug Administration (FDA) had granted UK-based OxfordVR a breakthrough device designation for its gameChangeVR treatment to deliver immersive cognitive behaviour therapy (CBT) to people suffering from schizophrenia and other mental illnesses.

Food and Drug Administration 141

Food and Drug Administration Pharmacology Side effects Physicians 141

Legacy MEDSearch

JANUARY 3, 2023

Food and Drug Administration for its Respiratory Health point of care test. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Visby Medical announced that it has received Emergency Use Authorization (EUA) from the U.S. About Visby Medical.

Medical 98

Medical Food and Drug Administration FDA Recruitment 98

Legacy MEDSearch

FEBRUARY 13, 2023

Food and Drug Administration (FDA) 510(k) clearance and launch of the company’s upgraded AI-powered software. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. Hyperfine, Inc., The Swoop® system received initial U.S.

Food and Drug Administration 98

Food and Drug Administration FDA Recruitment Food 98

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 Food 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

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

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. See Full Press Release at the Source: ABM RESPIRATORY CARE ANNOUNCES THE FDA CLEARANCE OF THE BIWAZE CLEAR SYSTEM.

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 12, 2022

Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. The post IRRAS Receives US FDA 510(k) Clearance for its Next Generation IRRAflow Control Unit appeared first on Legacy MedSearch | Medical Device Recruiters. Press Release by: IRRAS.

FDA 95

FDA Food and Drug Administration Recruitment Medical 95

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. See Full Press Release at the Source: Inspira Technologies Begins Manufacturing of the ALICE CPB Device, ahead of planned 2023 FDA submission.

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

DECEMBER 7, 2022

Food and Drug Administration market clearance for the ArthroFree System. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. The company hit an important milestone in March 2022 when it received U.S. Press Release by: Lazurite.

Networking 98

Networking Medical Food and Drug Administration Recruitment 98

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. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. This is a proud day in Activ Surgical’s history.”. Press Release by: Activ Surgical.

Food and Drug Administration 98

Food and Drug Administration Safety Recruitment Medical 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. Press Release by: Tyber Medical. Contact us to discuss partnering with Legacy MedSearch on your position.

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

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

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., Press Release by: Aerin Medical.

Medical 98

Medical Patients FDA Physicians 98

Legacy MEDSearch

NOVEMBER 9, 2022

Food and Drug Administration. Legacy MedSearch has more than 35 years of combined experience recruiting in the medical device industry. The post Saranas Announces Over 1,200 Patients Treated with the Early Bird® Bleed Monitoring System appeared first on Legacy MedSearch | Medical Device Recruiters. 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., Press Release by: Medcura.

Food and Drug Administration 97

Food and Drug Administration FDA Recruitment Medical 97

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. Press Release by: HemoSonics, LLC. Contact us to discuss partnering with Legacy MedSearch on your position.

FDA 95

FDA Food and Drug Administration Recruitment Medical 95

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

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. Press Release by: Xironetic.

Food and Drug Administration 52

Food and Drug Administration FDA Recruitment Food 52

Pharmaceutical Technology

APRIL 19, 2023

While the Clarksville, US-based company completed a Phase Ia study in healthy participants to eventually develop the drug for Alzheimer’s disease, it is likely that the company will now focus on Parkinson’s disease in its Phase II study first, said Kelleher-Andersson. Similarly, research collaborations are also a consideration.

Food and Drug Administration 52

Food and Drug Administration Recruitment Prospecting Food 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

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. Press Release by: Cytovale.

Food and Drug Administration 98

Food and Drug Administration FDA Recruitment Medical 98