88 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HydroSens A (hioxifilcon A) Spherical Hydrogel Soft Contact Lens
FDA 510(k)
FDA Class 2
·Ophthalmic
Fuse ULTRA Foot plating System
FDA UDI
CPM Medical Consultants, LLC·B565R2006180·CONCAVE REAMER 18MM
Ceramco® iC
FDA UDI
Dentsply International Inc.·D00142006180·CC-001
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450190715·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694017619·MFx Tag, Auto-Drive Angulated Locking Screw, Blank
OsteoMed
FDA UDI
OSTEOMED LLC·00845694017640·MFx Tag, Auto-Drive Angulated Locking Screw, 6mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694017626·MFx Tag, Auto-Drive Angulated Locking Screw, 4mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694017657·MFx Tag, Auto-Drive Angulated Locking Screw, 8mm
OsteoMed
FDA UDI
OSTEOMED LLC·00845694017633·MFx Tag, Auto-Drive Angulated Locking Screw, 5mm
Apelo® / Apelo® MIS
FDA UDI
ATLAS SPINE, INC.·M68120061800000·Ratcheting In-Line Handle
AALTO SCIENTIFIC MIRCO HEMATOCRIT CONTROL
FDA 510(k)
FDA Class 2
·Hematology
SCANDINAVIAN IVF SCIENCES AB, THAW-KIT 1
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MEDTRONIC MINIMED
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code FPA·July 10, 2009
ITREL
FDA Adverse Event
Death
·MEDTRONIC NEUROMODULATION·Product code LNQ·August 19, 2008
ITREL
FDA Adverse Event
Death
·MEDTRONIC NEUROMODULATION·Product code LNQ·August 19, 2008
ITREL
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LNQ·August 8, 2008
ENTERRA THERAPY
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LNQ·April 28, 2008
ITREL
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LNQ·August 8, 2008
ITREL
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LNQ·August 8, 2008
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 16, 2024