35 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Dornier Medilas H Solvo 35 Laser
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Maestro™ Total Wrist
FDA UDI
Biomet Orthopedics, LLC·00887868239755·
MAESTRO TOTAL WRIST
FDA UDI
Biomet Orthopedics, LLC·00880304479524·
VARIABLE LOCK SCREW 4.75X35MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWJ·January 24, 2018
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K1103500·Tray, Base, 3.5", Arcamed
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197453080·CCR Titanium Lateral Blade
24x50m...
All Poly Monotrial
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063818·
KNEEHAB XP
FDA 510(k)
FDA Class 2
·Neurology
HOVEROUND TEKNIQUE GT POWER WHEELCHAIR, MODEL# TEKNIQUE GT
FDA 510(k)
FDA Class 2
·Physical Medicine
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·July 31, 2020
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·December 4, 2019
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·April 30, 2021
SURESTEP
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·October 28, 1998
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·August 31, 2020
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·February 21, 2019
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·September 16, 2022
T:SLIM G5 SYSTEM
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OYC·October 22, 2019
LOCKING SCREW, FULLY THREADED 5X55 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 30, 2010
ACCU-CHEK SPIRIT
FDA Adverse Event
Injury
·DISETRONIC MEDICAL SYSTEMS·Product code LZG·December 11, 2009
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 18, 2012