Medical Device Guru
@MedDeviceGurus
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With 25+ yrs in the #MedicalDevice industry, our #recruiting expertise extends to #sales, diagnostic & therapeutic #imaging, #engineering, & #robotics
Orlando, FL
Joined May 2009
Prolira Announces FDA Clearance of the DeltaScan® Brain State Monitor for Detecting Acute Encephalopathy (Acute Brain Failure), a Condition Affecting Millions of Hospitalized Patients 60 and Older
legacymedsearch.com
Prolira BV, a company committed to enabling early and effective treatment of patients at risk of developing acute brain failure, announced it has received 510(k) clearance from the FDA for the...
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HeartBeam Announces Acquisition of LIVMOR Assets
legacymedsearch.com
HeartBeam, Inc., a cardiac technology company that has developed the first and only 3D-vector electrocardiogram (VECG) platform for heart attack detection anytime, anywhere, announced the strategic...
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NanoVibronix Announces Positive Results from Independent Product Trial of UroShield for Patients with a Spinal Cord Injury
legacymedsearch.com
NanoVibronix, Inc., a medical device company utilizing the Company's proprietary and patented low intensity surface acoustic wave (SAW) technology, announced the positive evaluation results for its...
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Vivasure Medical Announces FDA IDE Approval to Initiate U.S. Pivotal Study
legacymedsearch.com
Vivasure Medical announced that the U.S. FDA has granted an Investigational Device Exemption (IDE) to advance the company’s PATCH Clinical Study, a multi-center, single-arm, pivotal study evaluating...
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Are you headed to #AAOS this year? Chris and Sean will be at the show ready to discuss your strategic talent needs for 2023! To request an appointment to meet with our team, click here: https://t.co/LqqFD56gIF
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Lumendi Receives 510(k) Clearance for Two New Devices
legacymedsearch.com
Lumendi, LLC announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for DiLumen EZ¹, a single-use, disposable endotherapy device for endoscopic mucosal resections...
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Hyperfine, Inc. Announces FDA Clearance for Improved AI-Powered Software and Expanded Field of View for the Swoop® Portable MR Imaging® System
legacymedsearch.com
Hyperfine, Inc., the groundbreaking medical device company that created the Swoop® system, the world’s first FDA-cleared portable magnetic resonance imaging (MRI) device for imaging of the brain,...
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Catalyst Receives FDA 510(k) Clearance for its Convertible Stemmed Total Shoulder Arthroplasty System
legacymedsearch.com
Catalyst OrthoScience Inc. (Catalyst), a medical device company focused on the upper extremity orthopedics market, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to...
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Globus Medical and NuVasive to Combine in All-Stock Transaction to Create Innovative Global Musculoskeletal Company Focused on Patient Care
legacymedsearch.com
Globus Medical, a leading musculoskeletal solutions company, and NUVASIVE (NASDAQ: NUVA), the leader in spine technology innovation, today announced they have entered into a definitive agreement to...
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CoolHealth Enters U.S. Market With TargetCool™, A Breakthrough FDA-Class II Medical Device Offering Unprecedented Precise, Rapid Cooling For Pain Management And Bruise Minimization
legacymedsearch.com
CoolHealth is entering the U.S. market with a breakthrough FDA-Class II medical device, TargetCool™. Leveraging groundbreaking, tuneable cooling technology, TargetCool rapidly cools the skin allowing...
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Candela Introduces the New FDA-Cleared Profound Matrix™ System
legacymedsearch.com
Candela, the leading provider of energy-based solutions worldwide, and the pioneer of the first and only long-pulse radiofrequency (RF) microneedling device, announces the launch of the all-new...
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RefleXion Receives FDA Clearance for SCINTIX Biology-Guided Radiotherapy; Cutting-edge Treatment Applicable for Early and Late-stage Cancers
legacymedsearch.com
RefleXion Medical, a therapeutic oncology company, announced the U.S. Food and Drug Administration (FDA) has granted the first marketing clearance for its SCINTIX™ biology-guided radiotherapy, a...
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VERO Biotech's Second Generation GENOSYL® Delivery System (DS) Receives FDA Approval in Anesthesia in the Surgical Suite
legacymedsearch.com
VERO Biotech Inc., a commercial-stage healthcare business dedicated to neonatal intensive care and the acute care hospital community, announced FDA approval of its innovative second generation...
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Axonics Receives FDA Approval for Fourth-Generation Rechargeable Sacral Neuromodulation System
legacymedsearch.com
Axonics, Inc., a global medical technology company that is developing and commercializing novel products for the treatment of bladder and bowel dysfunction, announced that the U.S. Food and Drug...
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Opportunity with a highly competitive spine organization in the Midwest! To learn more, reach out to Sean, or click here: https://t.co/E8YqTm2PeB
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#newopportunity! Quality Engineer role in Georgia with a great #MedTech start-up! To learn more or apply, click here: https://t.co/vyHKqPsEZn
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Able Medical Announces Launch of Valkyrie® Looped Sternotomy Sutures
legacymedsearch.com
Able Medical Devices announced the launch of Valkyrie® Looped Sternotomy Sutures. When compared to traditional wire sutures, the Valkyrie Looped Suture doubles the surface area of single wires and...
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#newopportunity! Our client is looking for an Account Manager on the West Coast to join their team! Learn more here: https://t.co/W7KrxfTvvh
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