25 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DC-70/DC-70T /DC-70 Pro/DC-70 Exp/DC-75/DC-78/DC-70S Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
M2A MODULAR HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304209268·
COLIN PRESS MATE, MODEL BP S510
FDA 510(k)
FDA Class 2
·Cardiovascular
GE LOGIQ I, LOGIQ E AND VIVID E
FDA 510(k)
FDA Class 2
·Radiology
MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S6 RM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSX·January 17, 2022
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 25, 2025
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 11, 2013
GYNECARE X-TRACT MORCELLATOR
FDA Adverse Event
Malfunction
·ETHICON·Product code HET·July 15, 2011
CONTOUR TEST STRIPS (50)
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC.·Product code NBW·September 9, 2008
Merit Inflation Syringe Kit. Catalog Number KOS-02857
FDA Recall
Terminated
·Merit Medical Systems, Inc.·Product code MAV·August 25, 2016
UNKNOWN SHELL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·August 14, 2017
M2A TPR HI CARBON 41/32MM LNR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWY·February 23, 2018
FLEXCATH ADVANCE STEERABLE SHEATH
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code DRA·July 17, 2017
ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code OAE·July 17, 2017
ACHIEVE MAPPING CATHETER
FDA Adverse Event
Injury
·MEDTRONIC MEXICO·Product code DRF·July 17, 2017
MOTO PARTIAL KNEE TIBIAL TRAY FIX CEMENTED S7 RM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code HSX·October 10, 2018
MODULAR TAPERLOC FEMORAL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·August 14, 2017
UNKNOWN LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·August 14, 2017
M2A-T M/H RAD 2HL SHL 41/54MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 23, 2018
M2A TAPER LINER
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWY·August 17, 2017