SELUTION SLR™ wins historic US FDA nod for in‑stent restenosis
SELUTION SLR™ wins historic US FDA nod for in‑stent restenosis The US Food and Drug Administration has approved the SELUTION SLR™ (Sustained Limus Release) Drug-Eluting Bal...
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SELUTION SLR™ wins historic US FDA nod for in‑stent restenosis The US Food and Drug Administration has approved the SELUTION SLR™ (Sustained Limus Release) Drug-Eluting Bal...
ISSCA's most comprehensive credential to date integrates regenerative medicine, biotechnology, longevity medicine, and artificial intelligence - a durable, multi-year physician-rel...
Engagement with leading orthopedic surgeons and cartilage repair specialists highlights growing awareness of GelrinC's off-the-shelf regenerative technologyGelrinC is CE Mark appro...
Medtronic announced the FDA has cleared the LigaSureв„ў RAS Maryland jaw device for use with the Hugoв„ў robotic-assisted surgery (RAS) system.
GALWAY, Ireland, Sept. 16, 2026 /PRNewswire/ — Medtronic (NYSE: MDT), a global leader in healthcare technology, today announced the U.S. Food and…
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