53 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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QUANTA SYSTEM DUOLITE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
RingLoc® Hip System
FDA UDI
Biomet Orthopedics, LLC·00880304185746·
Neodent
FDA UDI
JJGC Indústria e Comércio de Materiais Dentários S/A.·07899878047094·NGS REGULAR TAPERED DRILL
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964083983·Endo Carry-On Procedure Kit
SELF CENTERING
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295003298·SELF CENTERING BI-POLAR HEAD 28mm ID 39mm OD
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964074691·Endo Carry-On Procedure Kit
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964074806·Endo Carry-On Procedure Kit
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964077647·Endo Carry-On Procedure Kit
ROSSMAX MEDIPRO, MODELS 100F, 200F, AND 300F BLOOD PRESSURE MONITORS
FDA 510(k)
FDA Class 2
·Cardiovascular
PREVENTECH PROPHYLAXIS PASTE WITH FLUORIDE
FDA 510(k)
FDA Class 1
·Dental
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973530·
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC·Product code OTN·May 9, 2013
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code MTA·September 19, 2014
MACH1 GUIDE CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·May 26, 2011
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·August 8, 2025
ARCOS 19X190MM SPL TPR DIST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 14, 2018
TI LOW PROFILE SCREW 6.5X50MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018
TI LOW PROFILE SCREW 6.5X45MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 27, 2018
VANDUYNE RIGHT TRIFLANGE SZ 25
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·February 27, 2018
TI LOW PROFILE SCREW 6.5X50MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·March 13, 2018