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Medtronic Reports Second Quarter Financial Results

DUBLIN, Nov. 19, 2019 (GLOBE NEWSWIRE) —  Medtronic plc (NYSE:MDT) today announced financial results for its second quarter of fiscal year 2020, which ended October 25, 2019. The company reported second quarter worldwide revenue of $7.706 billion, an increase of 3.0 percent as reported or 4.1 percent on an organic basis, which adjusts for a $97 million negative impact …

New study shows 96% healing of hard to treat large and massive rotator cuff tears with Smith+Nephew’s REGENETEN™ Bioinductive Implant

LONDON, Nov. 19, 2019 /PRNewswire/ — Smith+Nephew (LSE: SN,NYSE: SNN), the global medical technology business, today announces a new clinical study illustrating the successful treatment of large (3-5cm) and massive (5cm+) rotator cuff tears using its REGENETEN Bioinductive Implant.1 Repairs of large and massive rotator cuff tears are recognised as having a high rate of failure, with more …

State-of-the-Art Spine Surgery Technology Makes Debut at Northwest Specialty Hospital

POST FALLS, Idaho, Nov. 19, 2019 /PRNewswire/ — Northwest Specialty Hospital is the first hospital in the Pacific Northwest to offer a combination of innovative robotic technology and automation for spine surgery that has earned it the distinction of becoming a nationally recognized surgical observation center for spine procedures. Northwest Specialty Hospital has quietly been earning national recognition …

SINTX Technologies Releases 2019 Third Quarter and Year-To-Date Earnings Report and Provides Business Update

SALT LAKE CITY, UT, Nov. 18, 2019 (GLOBE NEWSWIRE) — SINTX Technologies, Inc. (NASDAQ: SINT) (the “Company”), an original equipment manufacturer (OEM) ceramics company that develops and commercializes silicon nitride for medical and non-medical applications, today announced financial results for the three and nine month periods ended September 30, 2019 and provided a business update. …

Cerapedics Announces FDA Approval of PMA Supplement Based on Two-Year Clinical Data

WESTMINSTER, Colo., Nov. 18, 2019 /PRNewswire/ — Cerapedics, a private ortho-biologics company, today announced the U.S. Food and Drug Administration (FDA) has approved the company’s Premarket Approval (PMA) supplement for i-FACTOR Peptide Enhanced Bone Graft in anterior cervical discectomy and fusion (ACDF) procedures in patients with degenerative cervical disc disease. Cerapedics requested approval for an updated package …

Two of the first M6-C™ Artificial Cervical Disc Implantations Performed in the U.S. Take Place at Hudson Regional Hospital

SECAUCUS, NJ, November 18, 2019—Surgeons have performed only a few M6-C™ artificial cervical disc implantation surgeries in The United States since it was approved by the FDA in January 2019, with New Jersey’s first one performed at Hudson Regional Hospital by Dr. Jonathan Lewin on Sept. 10th and the second one by Dr. Fabien Bitan …

World’s First “Artificial Meniscus” Available in Israel

MEMPHIS, Tenn. – November 18, 2019 – Active Implants LLC, a company that develops orthopedic implant solutions, today announced that two patients in Israel have undergone knee surgery for the company’s NUsurface® Meniscus Implant – the first “artificial meniscus” to be marketed in the Middle East. Until now, the NUsurface Implant was only available in …

Biedermann Motech Announces Publication Of Initial Clinical Outcome Data On Mini-Open, Microsurgical iMAS360™ Procedural Solution For The Lumbar Spine

MIAMI/SCHWENNINGEN –(BUSINESS WIRE)–Biedermann Motech, the leader in pedicle screw technology and pioneer in the spinal market for more than 30 years, today announced the publication of initial clinical data in relation to its iMAS360 Procedure. The abstract with the title “Evaluation of the safety and feasibility of a new interpedicular microinvasive surgical technique (iMAS) for …

OrthoPediatrics Corp. Announces U.S. Launch of PediFoot Deformity Correction System

WARSAW, Ind., Nov. 15, 2019 (GLOBE NEWSWIRE) — OrthoPediatrics Corp. (“OrthoPediatrics”) (NASDAQ: KIDS), a company focused exclusively on advancing the field of pediatric orthopedics, is pleased to announce the domestic launch of the PediFoot Deformity Correction System (“PediFoot”), following 510(k) clearance by the U.S. Food and Drug Administration (FDA) in August. The PediFoot system is the first …

SANUWAVE Health Reports Third Quarter 2019 Financial Results

SUWANEE, Ga., Nov. 15, 2019 (GLOBE NEWSWIRE) — SANUWAVE Health, Inc. (OTCQB: SNWV) reported financial results for the three and nine months ended September 30, 2019 with the SEC on Thursday, November 14, 2019. The Company will also host a conference call today, November 15, 2019, at 9:00 a.m. Eastern Time.  Highlights from the third quarter and last …

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