22 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT
FDA 510(k)
FDA Class 2
·Neurology
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690185413·Revision Knee Spiral Reamer- Hudson Short Flute...
JOBST forMen
FDA UDI
BSN MEDICAL, INC.·04042809842463·FOR MEN 30-40 MM HG KNEE HIGH CLOSED TOE LARGE ...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197383271·FOERSTER Sponge Forceps
250mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197533041·Vascular DeBakey Forceps
Ø5mm, ...
GORE-TEX VASCULAR GRAFT; GORE-TEX STRETCH VASCULAR GRAFT
FDA 510(k)
FDA Class 2
·Cardiovascular
FMP METAL/METAL ACETABULAR INSERT
FDA 510(k)
FDA Class 3
·Orthopedic
EXC ABT RNGLC-X SHELL PC 050MM DIA50MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·February 21, 2018
DELTA CER FEM HD 32/0MM T1 M T1
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·February 21, 2018
UNIV 2-HOLE SHL 50MM LNR SZ 23
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code LPH·February 13, 2018
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·April 11, 2013
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·May 28, 2008
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·April 13, 2011
RINGLOC HIP SYSTEM 2 HOLE ACETABULAR SHELL UNIVERSAL WITH APICAL DOME HOLE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·July 6, 2017
SIRIUS HIP STEM 38-C
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·February 15, 2018
VANGUARD XP-XP TIBIAL TRAY INTERLOK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·January 5, 2018
VANGUARD XP FEMORAL LEFT WITH PEGS
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·January 5, 2018
VANGUARD XP-XP LEFT LATERAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBH·January 5, 2018
RLOC-X ARCOMXL H/W 50/32MM 23
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code LPH·July 13, 2020
ACCUSCREEN ABR/DP TYPE 1077
FDA Adverse Event
Malfunction
·NATUS MEDICAL DENMARK APS·Product code GWJ·October 26, 2022