8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MYELOTEC MYELOSCOPE
FDA 510(k)
FDA Class 2
·Orthopedic
StarFuse Interphalangeal Pin
FDA 510(k)
FDA Class 2
·Orthopedic
MARCH HEALTHCARE HEALTH MONITORING KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
ATTUNE CR FB INSRT SZ 7 10MM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·December 29, 2021
LAUREATE WORLD PHACO SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 24, 2014
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER·Product code HQC·August 3, 2015
OT VERIO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 14, 2013
Exactech Equinoxe REVERSE SHOULDER, 38mm Humeral Liner: a) +0mm, Item Number 320-38-00, b) +2.5mm, Item Number 320-38-03; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024