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BioWorld - Monday, June 15, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Sep. 26, 2022

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Clearpoint

Clearpoint’s Swedish partner snares 510(k) for laser interstitial therapy for brain lesions

Clearpoint Neuro Inc. said Clinical Laserthermia Systems AB (CLS), snared a 510(k) from the FDA for a laser interstitial therapy system that will be marketed in the U.S. as part of the Clearpoint Prism Neuro system. This product package adds to a growing Clearpoint footprint in the neurological disorders space, adding to an inventory that already consists of targeted drug delivery and deep brain stimulation systems. Read More
Ciliatech CID concept

Ciliatech eyes new future in glaucoma treatment

A new technique may allow reduction of intraocular pressure (IOP) associated with glaucoma without opening the anterior eye chamber, eliminating much of the risk associated with current glaucoma procedures. The cilio-scleral inter-position device (CID) facilitates outflow without creating an artificial egress using a thin one-piece implant. Read More
Boston Scientific - Watchman FLX

Dueling trials highlight differences between Amulet and Watchman LAA closure devices

Boston Scientific Corp. and Abbott Laboratories continue to parry over clinical trials comparing the latter’s Amplatzer Amulet with Boston Scientific’s Watchman in sealing the heart’s left atrial appendage (LAA) to prevent ischemic stroke in patients with atrial fibrillation (Afib). In one of five presentations at the 34th Transcatheter Cardiovascular Therapeutics annual scientific symposium in Boston in mid-September, Abbott said device-related thrombosis or peri-device leak more frequently preceded strokes in patients with Watchman compared to those with Abbott’s Amplatzer Amulet device. Read More
Ecential Robotics - surgical assistance robot

Ecential Robotics awarded FDA clearance for its robotic platform for spine surgery

Ecential Robotics SAS reported U.S. FDA 510(k) clearance for its 3D imaging, navigation and robotics guidance system. Read More
deal2.png

Senate, House committees work to avert FDA shutdown with user fee handshake

Legislation to reauthorize a number of U.S. FDA user fee programs has once again languished until the 11th hour, but the House and Senate committees of jurisdiction have apparently come to terms over the matter. However, the parties to this deal are characterizing it as a “clean” bill, which suggests that FDA regulation of lab-developed tests (LDTs) and a center of drug manufacturing of excellence will have to wait for another day or – because of the upcoming mid-term elections – most likely another year. Read More

US FDA lays out safeguards for including kids in trials

In recent years, ethicists have executed a 180-degree shift on including children in clinical trials testing drugs, biologics and medical devices, moving from the idea that it was unethical to include youngsters in trials to an understanding that such inclusion may be the best way of protecting them. Read More

Med-tech gainers and losers for Sept. 19-23, 2022

The top 10 med-tech stock gainers and losers for the week. Read More

Appointments and advancements for Sept. 26, 2022

New hires and promotions in the med-tech industry, including: Tissium, Titan Medical. Read More

Financings for Sept. 26, 2022

Med-tech firms raising money in public or private financings, including: Surge. Read More

In the clinic for Sept. 26, 2022

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Creative Medical Technology. Read More

Other news to note for Sept. 26, 2022

Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Biocartis, Immunovia. Read More

Regulatory actions for Sept. 26, 2022

Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Clearpoint Neuro, Precisis, Pulse Biosciences. Read More

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