33 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TiWAVE-C Porous Titanium Cervical Cage
FDA 510(k)
FDA Class 2
·Orthopedic
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526768451·GENUMEDI PSS GREEN I
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486002541·MCK Patellofemoral Component
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668100943·JAFFE LID RETRACTOR SMALL
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·April 29, 2018
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·April 29, 2018
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·April 28, 2018
Suzy Holemaker
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215063771·
N/A
FDA UDI
Ortho Development Corporation·00822409128891·4-in-1 Cut Guide w/ Anterior Lip Size 1
SHELL CAGE, WAVE CAGE, LOOP CAGE
FDA 510(k)
FDA Class 2
·Orthopedic
SWERV MAGNETOSTRICTIVE ULTRASONIC SCALER SYSTEM
FDA 510(k)
FDA Class 2
·Dental
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/10 MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·May 28, 2019
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/10 MM L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·September 19, 2022
SYRINGE 5ML LL BNS
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·September 29, 2021
IRRIGATION TUBING
FDA Adverse Event
Malfunction
·CODMAN & SHURTLEFF, INC·Product code GEI·January 16, 2015
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011
ADVANTAGE SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013
CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·October 17, 2014
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code PQF·April 29, 2018
MK-2000
FDA Adverse Event
Injury
·NIDEK CO., LTD.·Product code HNO·November 14, 2019