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BioWorld - Wednesday, April 15, 2026
Home » Topics » Medical technology

Medical technology
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U.S. Securities and Exchange Commission

Jury agrees with SEC’s ‘shadow trading’ allegations

April 8, 2024
By Mari Serebrov
A quick jury verdict that a biopharma official was guilty of insider trading validated the U.S. SEC’s broader view of what constitutes such trading and could ignite more SEC “shadow trading” investigations and allegations. Following an eight-day trial before the U.S. District Court for the Northern District of California and a little more than two hours of deliberation, a jury found April 5 that Matthew Panuwat violated national securities laws when he purchased short-term, out-of-the-money stock options in Incyte Corp. in 2016.
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Med-tech gainers and losers for April 1-5, 2024

April 8, 2024
The top 10 med-tech stock gainers and losers for the week.
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Regulatory actions for April 8, 2024

April 8, 2024
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Onkos Surgical, Spirair, Venus Concept.
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Other news to note for April 8, 2024

April 8, 2024
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Asept, Boston Scientific, Gopath, MMI, Nucleai, Sansure, Sepsmart, Spinex.
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In the clinic for April 8, 2024

April 8, 2024
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Medtronic, Natera, Precoridor, Seekin, V-Wave.
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Appointments and advancements for April 8, 2024

April 8, 2024
New hires and promotions in the med-tech industry, including: Clario, Sanara, Solesis.
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ihealthscreen
Patents

Ihealthscreen issued further patent for its AI eye screening system

April 8, 2024
By Simon Kerton
Richmond Hill, N.Y.-based Ihealthscreen Inc. reported the granting of a patent from the USPTO for automated systems for predicting and detecting the onset of glaucoma.
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Product recall concept image

J&J’s Medos withdrawing neurovascular guide catheters

April 8, 2024
By Mark McCarty
The U.S. FDA announced a class I recall of single-use neurovascular guide catheters made by Medos International Sarl SA of Neuchatel, Switzerland, because of fractures in the device’s distal catheter shaft. The FDA stated that the issue, seen in the company’s Cerebase DA line of guide sheaths, has led Medos to recommend that customers quarantine any of the affected devices, although a root cause has not yet been identified.
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Gavel and FTC logo

USTR’s Tai sees state champions as anticompetitive policy instruments

April 8, 2024
By Mark McCarty
Life science companies and the Office of the U.S. Trade Representative have not always seen eye to eye on issues such as compulsory licensing, but industry might be supportive of a remark by U.S. Trade Representative Katherine Tai about companies that are provided with anticompetitive breathing by their host governments with noticeable anticompetitive effect. 
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spirair septalign

It’s Spirair by a nose as Septalign gains FDA clearance

April 8, 2024
By Annette Boyle
Spirair Inc. won the race for the first U.S. FDA 510(k) clearance for a minimally invasive therapy for nasal septal deviation (NSD), the company said. The Septalign system features a bioabsorbable implant that enables minor cartilaginous septal deviation that can be placed in an office with local anesthesia.

“Traditional septoplasty and septorhinoplasty can require significant time away from work, with nearly 42% of patients requiring two weeks or more for recovery. With Septalign, recovery is much faster and requires little to no time away from work for recovery,” Spirair CEO Ben Bishop told BioWorld.
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