Activ Surgical Announces FDA Clearance for ActivSight Intraoperative Imaging Module

Activ Surgical announced the U.S. Food and Drug Administration (FDA) 510(k) clearance of the company’s ActivSight Intraoperative Imaging Module for enhanced surgical visualization.

Metrex Surface Disinfectant Portfolio Secures EPA Approval

The U.S. Environmental Protection Agency (EPA) has approved all eight surface disinfectant products made by an infection prevention leader, Metrex, as effective against SARS-CoV-2, the novel coronavirus that causes COVID-19.

Olympus Supports Safety Actions Regarding Surgical Smoke

Olympus has announced its support of The Joint Commission’s recommended safety actions for managing the hazards of exposure to surgical smoke for health care staff in operating rooms.

Exofin Fusion Redesign Receives FDA Approval

Chemence Medical, a leader in medical cyanoacrylate devices and products, announced the U.S. Federal Drug Administration’s (FDA) 510(k) approval of the company’s redesigned exofin fusion skin closure system.

Abstracts Invited for ASTM International Virtual Workshop on Fast-Tracking PPE Standards Development

Abstracts for presentation are invited for the ASTM International virtual workshop on Fast-Tracking Standards Development to Address Personal Protective Equipment (PPE) Shortages Due to the COVID-19 Pandemic, Sept. 9-10, 2020. ASTM International’s committees on medical and surgical materials and devices (F04) and personal protective clothing and equipment (F23) will be co-sponsoring the virtual workshop.

The objectives of the workshop are to leverage efforts to alleviate PPE shortages and identify subjects for new standards that address shortages for the current pandemic and possible future outbreaks. This workshop will provide a forum for engineers, scientists, and medical professionals worldwide to exchange ideas and identify areas for needed standard development.

Topics for discussion include:

  • current issues with decontaminating single use PPE,
  • cleaning, decontamination, and sterilization,
  • assessing the performance of devices and device components in short supply,
  • current standards being used and more.

To participate in the workshop, authors must submit a 300-word abstract clearly identifying new standards or revisions to existing standards needed. Please email the abstract for consideration to no later than July 26, 2020.

Additional technical information is available from the workshop chairs. For more information on the workshop, please visit



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