34 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TELIX K Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507
FDA 510(k)
FDA Class 2
·Neurology
VARIAN HIGH ENERGY LINEAR ACCELERATOR
FDA 510(k)
FDA Class 2
·Radiology
M-VIZION FEMORAL REVISION SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·November 5, 2025
BALL HEADS: COCR 01.25.012 COCR BALL HEAD 12/14 Ø 28 SIZE M 0
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·April 14, 2023
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 23, 2013
ACCU-CHEK RAPID-D LINK INFUSION SET
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FPA·June 22, 2011
COLLEAGUE 3CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 24, 2008
STEM: M-VIZION 01.22.102 DISTAL STEM 13MM L 140MM STRAIGHT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·October 1, 2021
M-VIZION FEMORAL REVISION SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·October 2, 2025
OPTETRAK LOGIC
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 27, 2023
M2A 38MM MOD HD +3MM NK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LZO·November 12, 2019
REGEN/RNGLC+ MULTI 58MM SZ 24
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 12, 2019
M-VIZION FEMORAL REVISION SYSTEM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·November 21, 2024
E-POLY 38MM +5HW LNR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code OIY·November 12, 2019
LOGIC KNEE COMPONENTS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 13, 2023
M-VIZION PROXIMAL BODY Ø20MM L 70MM LAT
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·August 22, 2024
MPACT ACETABULAR SHELL Ø54 TWO-HOLES
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·December 20, 2023
ANSWER 9X125 COCR LAT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDG·April 29, 2022
PT HYBRID GLEN POST REGENEREX
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·December 5, 2022