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LifeVac receives FDA De Novo classification for anti-choking device
LifeVac is approved for use as a single-use, non-powered, non-invasive airway clearance device.
LONDON--(BUSINESS WIRE)--Technavio has announced the top five leading vendors in their recent global medical suction devices market report until 2021. This research report also lists five other ...
LifeVac has picked up a groundbreaking clearance from the FDA for its suction-powered device designed to dislodge an object ...
New breast implant suction retrieval device designed to help plastic surgeons efficiently remove ruptured breast implants while helping reduce silicone spillage BRECKSVILLE, Ohio, Feb. 25, 2026 ...
The Zucker Institute for Applied Neurosciences, a technology accelerator embedded in the Medical University of South Carolina, has partnered with Medical Access Partners, LLC to commercialize a ...
FDA-cleared suction retrieval device designed to streamline breast implant removal and reduce mess, handling, and operating time. BRECKSVILLE, Ohio, Feb. 12, 2026 /PRNewswire/ -- Applied Medical ...
HYDERABAD, India, Jan. 23, 2026 /PRNewswire/ -- According to Mordor Intelligence's latest report, the medical suction devices market is valued at USD 19.59 billion in 2026, and is projected to surpass ...
LifeVac LLC announced today that the U.S. Food and Drug Administration (FDA) has granted De Novo classification for LifeVac under 21 CFR 874.5400, formally establishing the device type "suction ...
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