24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Straumann BoneCeramic
FDA 510(k)
FDA Class 2
·Dental
HHM
FDA UDI
Oticon A/S·05707131353399·G400 S, MINIRITE T 312 2.4G C093 HHM
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019378·HPS 1.2mm Screw & Plate Module
Anti-Glutamate receptor (type NMDA) IFA
FDA UDI
EUROIMMUN Medizinische Labordiagnostika AG·04049016092575·
ANNULOFLO SYSTEM, MITRAL MODEL AR700
FDA 510(k)
FDA Class 2
·Cardiovascular
RX EVEREST
FDA 510(k)
FDA Class 2
·Dental
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523141487·SL Universal Acetabular Trial Shell, 51mm
FIREBIRD SFS
FDA Adverse Event
Malfunction
·ORTHOFIX INC.·Product code LXH·May 17, 2017
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024496163·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024496170·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024496156·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024496200·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024496194·
Stablecut®
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024496187·
ANCURE ENDOGRAFT (FORMERLY EVT ENDOGRAFT)
FDA Adverse Event
Injury
·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·May 3, 2011
BD PLASTIPAK¿ SYRINGES
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·June 14, 2023
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·October 27, 2014
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·July 1, 2011
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 2, 2013
BD PLASTIPAK¿ LUER-LOK¿ SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·June 18, 2022