Arthroscopy

FDA Clears Catalyst OrthoScience Reverse Shoulder System

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FDA Clears Catalyst OrthoScience Reverse Shoulder System

Catalyst OrthoScience Inc., a medical device company focused on the upper extremity orthopedics market, has received clearance from the U.S. Food & Drug Administration (FDA) to market its reverse shoulder system. Catalyst’s reverse shoulder system is a single-tray arthroplasty system that is made to combine beneficial and evidence-based attributes of reverse shoulder arthroplasty design. The

iData ResearchFDA Clears Catalyst OrthoScience Reverse Shoulder System
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Osso VR Partnering with MicroPort Orthopedics to Provide VR Training Module for Hip and Knee System

Osso VR Partnering with MicroPort Orthopedics to Provide VR Training Module for Hip and Knee System

Osso VR has been providing a virtual surgical training platform to provide an education to medical students who are currently unable to receive in-person training due to COVID-19. They have recently partnered with MicroPort Orthopedics, to provide students with an opportunity to take part in VR training of the surgical techniques used by MicroPort. The

iData ResearchOsso VR Partnering with MicroPort Orthopedics to Provide VR Training Module for Hip and Knee System
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Anika Releasing Six New FDA-Approved Sports Medicine Products in 2020

Anika Releasing Six New FDA-Approved Sports Medicine Products in 2020

Anika, an orthopedic device manufacturer based out of Bedford, Massachusetts, has announced the release of six new sports medicine products in 2020. This marks the first time Anika has released new products since acquiring Parcus Medical and Arthrosurface earlier in the year. All six of these products have received FDA approval. They are mainly focused

iData ResearchAnika Releasing Six New FDA-Approved Sports Medicine Products in 2020
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Integrated Endoscopy Global Launch of Arthroscope

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Integrated Endoscopy Global Launch of Arthroscope

Irvine-based Integrated Endoscopy has begun global distribution of their FDA-cleared NUVIS single-use, HD, battery operated arthroscope. Their low-cost endoscope is the first offering of its kind in the market for arthroscopic surgeries in the United States. The unique selling point of the NUVIS single-use arthroscope is that it alleviates any issues related to safety and

iData ResearchIntegrated Endoscopy Global Launch of Arthroscope
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Top Arthrex Competitors

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Top Arthrex Competitors

Register to receive a free synopsis and brochure. Browse the Report Library. Arthrex is a global medical company focused in orthopedic product development and education, and was founded in 1981. Today it is a privately held organization headquartered in Southwest Florida. Arthrex has an additional global division in Germany and several subsidiaries and distribution centers in Europe,

iData ResearchTop Arthrex Competitors
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Top ConMed Competitors in the United States

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Top ConMed Competitors in the United States

Register to receive a free synopsis and brochure. Browse the Report Library ConMed’s history began in 1970, when they were first established by Eugene Corasanti in Utica, New York as Consolidated Medical Equipment, Inc. Today, it is a leading global medical technology company in the United States. The business operates in a range of categories, including: arthroscopy,

iData ResearchTop ConMed Competitors in the United States
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Stryker Announces New Visualization Platform for Arthroscopy

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Stryker Announces New Visualization Platform for Arthroscopy

Register to receive a free U.S. Market Report Suite for Arthroscopic Devices – MedSuite report synopsis and brochure Stryker, a prominent market figure in the arthroscopic device industry, has introduced a new line of transformative visualization tools in their arthroscopy department. The platform, including the HipCheck, HipMap, 1688 Advanced Imaging Modalities (AIM) 4K Visualization Platform and Connected OR

iData ResearchStryker Announces New Visualization Platform for Arthroscopy
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Medtronic Gains FDA Clearance for Nerve Ablation Device

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Medtronic Gains FDA Clearance for Nerve Ablation Device

Register to receive a free U.S. Market Report Suite for Arthroscopic Devices – MedSuite report synopsis and brochure Medtronic has announced that they have recently gained 510(k) clearance from the U.S. Food and Drug Administration (FDA) for their Accurian radiofrequency nerve ablation device for treating chronic pain. Radiofrequency ablation is a minimally invasive procedure in which radio waves

iData ResearchMedtronic Gains FDA Clearance for Nerve Ablation Device
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Smith & Nephew Acquires Ceterix® Orthopaedics, Inc, the Developer of the NovoStitch® Pro Suture Passer

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Smith & Nephew Acquires Ceterix® Orthopaedics, Inc, the Developer of the NovoStitch® Pro Suture Passer

Register to receive a free U.S. Market Report Suite for Arthroscopic Devices – MedSuite report synopsis and brochure Smith & Nephew has announced its acquisition of Ceterix® Orthopaedics, Inc. for an initial $50 million and an additional $55 million over the next five years, depending on their financial performance. Ceterix Orthopaedics is the developer and manufacturer of the

iData ResearchSmith & Nephew Acquires Ceterix® Orthopaedics, Inc, the Developer of the NovoStitch® Pro Suture Passer
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Lipogems’ Receives FDA Clearance For Microfragmented Adipose Tissue System

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Lipogems’ Receives FDA Clearance For Microfragmented Adipose Tissue System

Register to receive a free U.S. Market Report Suite for Arthroscopic Devices – MedSuite report synopsis and brochure Lipogems, a leader in medical technologies for orthopaedic physicians, announced U.S. Food and Drug Administration (FDA) clearance of the company’s Lipogems Microfragmented Adipose Tissue Transplant System.  Federal regulators have cleared the way for this exciting new device and technology to

iData ResearchLipogems’ Receives FDA Clearance For Microfragmented Adipose Tissue System
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