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Laparoscopy Procedure Articles & Analysis

10 news found

ReShape Lifesciences Receives FDA 510(k) Clearance for the GIBI HD Calibration Tubes for use in Gastric and Bariatric Procedures

ReShape Lifesciences Receives FDA 510(k) Clearance for the GIBI HD Calibration Tubes for use in Gastric and Bariatric Procedures

New Calibration Tubes, in Three Sizes, Will Simplify Gastric and Bariatric Procedures Including Laparoscopic Sleeve Gastrectomy, Gastric Bypass and Gastric Banding Company to Introduce Product at IFSO 2022 World Congress in August; Sales to Commence in September ReShape Lifesciences (Nasdaq: RSLS), the premier physician-led weight loss and metabolic health solutions company, today announced ...

ByMedtimo Inc


Palisade Bio (Nasdaq: PALI) Announces Analysis Demonstrating LB1148 Reduced The Extent And Severity Of Post-Surgical Intraabdominal Adhesions By 93%

Palisade Bio (Nasdaq: PALI) Announces Analysis Demonstrating LB1148 Reduced The Extent And Severity Of Post-Surgical Intraabdominal Adhesions By 93%

Data from Pooled-Analysis of Enteral Protease Inhibitor LB1148 Demonstrated 72% Reduction in the Risk of Adhesion Formation in Patients Undergoing Bowel Resection Surgery Company to Host Conference Call on Wednesday, March 16, 2022, at 8:30 a.m. EST Palisade Bio, Inc. (Nasdaq: PALI), a clinical stage biopharmaceutical company advancing therapies for acute and chronic gastrointestinal (GI) ...

ByPalisade Bio


Memic Innovative Surgery to Demonstrate Use of Hominis® Surgical System at AAGL 2021

Memic Innovative Surgery to Demonstrate Use of Hominis® Surgical System at AAGL 2021

“Hominis is unique as it combines the advantages of transvaginal surgery, the preferred approach for hysterectomy, with the visual facility of laparoscopy and the ergonomic capabilities of robotic surgery, fulfilling an unmet need and presenting significant benefits to both clinicians and patients,” said Dr. ...

ByMomentis Surgical, Inc. (formerly Memic Innovative Surgery)


Asensus Surgical Announces Shinmatsudo Central General Hospital in Japan to Initiate Senhance Robotic Surgical System

Asensus Surgical Announces Shinmatsudo Central General Hospital in Japan to Initiate Senhance Robotic Surgical System

The hospital’s surgical department offers a wide range of surgical specialities, with a focus on cardiovascular and gastrointestinal surgery, where it employs a variety of surgical solutions including open, laparoscopic, and robotically assisted procedures. About Asensus Surgical, Inc. Asensus Surgical, Inc. is digitizing the interface between the surgeon and patient to ...

ByAsensus Surgical US, Inc.


New View Surgical, Inc. Announces FDA Clearance of its VisionPort™ System for Minimally Invasive Surgery

New View Surgical, Inc. Announces FDA Clearance of its VisionPort™ System for Minimally Invasive Surgery

New View Surgical, Inc., a medical device company developing proprietary imaging and access technologies for minimally invasive surgery (MIS), announced today that it received 510(k) clearance from the U.S. Food and Drug Administration for its VisionPort™ System. The VisionPort™ imaging and access system simplifies laparoscopic procedures for hospitals and provides surgeon-controlled ...

ByNew View Surgical


Asensus Surgical Announces FDA Clearance in General Surgery

Asensus Surgical Announces FDA Clearance in General Surgery

“General surgery is, by far, the largest area of manual laparoscopy which can benefit from the precision and insight of Performance-Guided Surgery. ...

ByAsensus Surgical US, Inc.


Mauna Kea Technologies Receives FDA 510(k) Clearance of Cellvizio® with a Fluorescent Dye, Fluorescein, as Drug Device Combination

Mauna Kea Technologies Receives FDA 510(k) Clearance of Cellvizio® with a Fluorescent Dye, Fluorescein, as Drug Device Combination

The Cellvizio®100 series system with all its different Confocal Miniprobes™ is now cleared for use with the fluorescein dye to image blood flow in the microvasculature and capillaries Mauna Kea Technologies today announced that it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the Cellvizio® 100 series and all associated Confocal Miniprobes™ for ...

ByMauna Kea Technologies


Lumendi Receives 510(K) Clearance for Dilumen Ik Endolumenal Interventional Knife

Lumendi Receives 510(K) Clearance for Dilumen Ik Endolumenal Interventional Knife

Connecticut-based medical device innovator Lumendi, LLC (http://www.lumendi.com) has announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the DiLumen Ik™ Endolumenal Interventional Knife, a sterile, single-use, disposable monopolar electrosurgical device for cutting, dissecting, and cauterizing tissue within the digestive tract during endoscopic procedures. ...

ByLumendi Ltd.


New View Surgical, Inc. Closes Series A Round of Financing

New View Surgical, Inc. Closes Series A Round of Financing

New View Surgical, Inc., an emerging medical device company developing proprietary imaging and access technologies for minimally invasive surgery, announced that it closed its Series A Financing Round at $2.5 million. The financing was over-subscribed due to investor demand. New View Surgical will deploy the financing to complete the development of its VisionPort™ System, expand the ...

ByNew View Surgical


Plasma Surgical Announces Expanded Indications for Use for the PlasmaJet® Surgery System

Plasma Surgical Announces Expanded Indications for Use for the PlasmaJet® Surgery System

FDA 510(k) clearance for removal of soft tissue by vaporization offers additional utility for surgeons ROSWELL, Ga. – May 1, 2013 – Plasma Surgical, creator of the PlasmaJet®, an advanced energy medical device designed as a safe and effective alternative to traditional electrosurgery instruments, announced today that it has received 510(k) clearance from the U.S. Food and Drug ...

ByPlasma Surgical, Inc.

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