22 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Straumann PrefGel
FDA 510(k)
FDA Unclassified
·Unknown
Sklar®
FDA UDI
SKLAR CORPORATION·10649111100598·S E METZ STAND NLSON CVD 11"TC
REACH(R) FEMORAL PROVISIONAL
FDA UDI
Biomet Orthopedics, LLC·00880304307162·
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·June 15, 2021
ALP 501 RB PUMP SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
KARMA MANUAL WHEELCHAIR, MODEL BUDGET 800
FDA 510(k)
FDA Class 1
·Physical Medicine
T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code OZO·September 6, 2019
M2A MODULAR HEAD COMPNOENT 38MM HEAD DIAMETER STANDARD NECK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·June 13, 2017
PROMUS ELEMENT? PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 11, 2013
SIGMA STAB GVF INS 5 8MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC·Product code JWH·July 7, 2011
HARMONIC ACE 36 CM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 8, 2008
M2A 38MM MOD HD STD NK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 26, 2018
M2A-38 CUP 50MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 26, 2018
MALLORY/HEAD ALTERNATE BEARING SHELL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWZ·February 8, 2017
M2A MODULAR HEAD COMPONENT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·February 8, 2017
M2A 38 MM ONE-PIECE CUP 38MM X 52 O.D.
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·September 30, 2016
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 4, 2016
M2A MODULAR HEAD COMPONENT 32MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·February 3, 2015
M2A TAPER LINER 32MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·February 3, 2015
GMK-HINGE FEMORAL COMPONENT SIZE 2 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KRO·June 28, 2019