1,571 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Plasdent
FDA UDI
PLASDENT CORPORATION·D832MFDM1·Disposable Model Formers, Medium, Clear
Plasdent
FDA UDI
PLASDENT CORPORATION·D832MFDL1·Disposable Model Formers, Universal, Clear
Orthoquest
FDA UDI
Young Innovations, Inc.·00843471155479·Sample Niti Thermal Multi-Force D-Form 020X020
Plasdent
FDA UDI
PLASDENT CORPORATION·D832MFDAST601·Disposable Model Formers, 20 of Each Size
MODEL MF..D & MX..D PACEMAKER LEADS
FDA 510(k)
FDA Class 3
·Cardiovascular
KermaX-plus
FDA UDI
IBA Dosimetry GmbH·EIBA120160MFD0·KermaX Product family is designed to be install...
TEGO
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code FPA·January 16, 2017
TRANSPAC
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code DRS·December 15, 2016
TRANSPAC
FDA Adverse Event
Malfunction
·ICU MEDICAL, INC.·Product code DRS·December 15, 2016
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·May 1, 2019
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·November 4, 2019
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·April 17, 2017
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·June 22, 2018
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·June 9, 2017
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·April 2, 2019
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·July 9, 2019
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·October 18, 2019
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·September 11, 2017
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·September 29, 2020
IFUSE IMPLANT SYSTEM
FDA Adverse Event
Injury
·SI-BONE, INC.·Product code OUR·July 28, 2017