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.


The OER-Pro is designed to save time and space while improving efficiency for endoscope reprocessing. With 99 percent uptime, the OER-Pro simultaneously reprocesses two flexible endoscopes in less than 30 minutes, delivering automatic high-level disinfection, alcohol flushing and air purging of channels. The RFID management system automatically records scope serial and model numbers, operator ID, and time of reprocessing, freeing staff from manual input of data. Additionally, the 18 inch wide footprint allows for maximize use of space in the reprocessing room.

For information on the OER-Pro, visit

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