8 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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SU-POR Patient-Specific Cranial Implant, SU-POR Patient-Specific Facial Implant
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
K152468
FDA UDI
Shenzhen Vistar Medical Supplies Co.,Ltd.·96973521874184·Reusable NIBP cuff,Thigh,single tube, HP connector
GOOD NIGHT
FDA 510(k)
FDA Class 2
·Dental
PROMETAL HN86
FDA 510(k)
FDA Class 2
·Dental
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MPRI·Product code LWS·June 7, 2013
OXIMAX N-600 PULSE OXIMETER
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY TYCOHEALTH·Product code DQA·June 21, 2011
TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIC·Product code NIQ·August 28, 2008
Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025