Philips Issues Correction for Trilogy Evo Ventilators Following FDA Class I Recall
The Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.
Read MoreThe Food and Drug Administration identifies the software update and nebulizer restrictions as the most serious type of recall.
Read MoreApr 14, 2026 | Company News | 0 |
The medical technology company has agreed to be acquired by American Industrial Partners in an all-cash deal.
Read MoreApr 13, 2026 | Clearances | 0 |
The system is designed to improve workflow efficiency and safety during minimally invasive left-heart procedures.
Read MoreMar 19, 2026 | Regulations & Standards | 1 |
As MDSAP gains traction and FDA quality requirements align with ISO 13485, HTM teams have new ways to evaluate equipment reliability, serviceability, and long-term performance before purchase.
Read MoreThe Department of Veterans Affairs has issued a presolicitation for a contract to provide technical and professional support to biomedical engineering departments across VA medical facilities nationwide.
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