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FDA: Cranial Drill Recall

FDA: Cranial Drill Recall

Integra LifeSciences has issued a recall for the Codman disposable perforators due to risk of device disassembly. This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device...

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Getinge, Zimmer Biomet Announce ASC Partnership

Getinge, Zimmer Biomet Announce ASC Partnership

Global MedTech companies Getinge and Zimmer Biomet Holdings Inc., have announced a strategic partnership where Zimmer Biomet will distribute Getinge’s Operating Room (OR) capital products to its ambulatory surgery center (ASC) customers. This partnership creates a...

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