58 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FACIAL SPA
FDA 510(k)
FDA Class 2
·Neurology
ArgenZ HT+ 95x14 OM1
FDA UDI
ARGEN CORPORATION, THE·D818122711·Dental porcelain/ceramic restoration kit
HEX-FIX
FDA UDI
Smith & Nephew, Inc.·03596010069450·TITANIUM HALF PIN 5.0MM X 40MM
BECHERT LENS NUCLEUS ROTATOR
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013377·BECHERT LENS NUCLEUS ROTATOR ANGLED BLUNT FORME...
BECHERT LENS NUCLEUS ROTATOR
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896013339·BECHERT LENS NUCLEUS ROTATOR ANGLED BLUNT FORME...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613112479·Sims Uterine Curette, Size 6, Sharp, Malleable ...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613112431·Sims Uterine Curette, Size 5, Sharp, Malleable ...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613112318·Sims Uterine Curette, Size 2, Sharp, Malleable ...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613112400·Sims Uterine Curette, Size 4, Sharp, Malleable ...
Plateau V & Z
FDA UDI
Life Spine, Inc.·00190837073244·Plateau V Spacer, 11mm x 22mm x 11mm,7 degree
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613077815·Sims Uterine Curette, Size 1, Sharp, Malleable ...
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613077822·Sims Uterine Curette, Size 3, Sharp, Malleable ...
MODIFICATION TO AVALON CUP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
NON-CONTACT THERMOMETER
FDA 510(k)
FDA Class 2
·General Hospital
VERSAFITCUP CC TERMINAL CUP IMPACTOR
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code MEH·June 4, 2014
NA
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code LZO·December 4, 2014
ACETABULAR SHELL CC TRIO NO-HOLE Ø 50
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·April 20, 2018
VERSAFITCUP CC HIGHCROSS PE LINER
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·October 31, 2013
VERSAFITCUP FLAT PE HC LINER Ø 36 / E
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code LZO·April 26, 2017
RESTORE ULTRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 21, 2013