31 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MOR Implant System
FDA 510(k)
FDA Class 2
·Dental
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100226·THORLAKSON ASPIRATING SPECULUM
DS CASSETTE
FDA 510(k)
FDA Class 2
·Radiology
VITOSS BA BIMODAL BIOACTIVE BONE GRAFT SUBSTITUTE
FDA 510(k)
FDA Class 2
·Orthopedic
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473171·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473218·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473232·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473188·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473126·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473164·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473195·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473201·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473225·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473140·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473157·
Persona Total Knee System
FDA UDI
Zimmer, Inc.·00889024473133·
GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)
FDA Adverse Event
Malfunction
·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018
SPRINT QUATTRO
FDA Adverse Event
Malfunction
·MPRI·Product code LWS·June 8, 2013
POLYFLUX S CAPILLARY DIALYZER
FDA Adverse Event
Malfunction
·GAMBRO DIALYLSATOREN GMBH·Product code KDI·September 4, 2008
UKNOWN ZIMMER KNEE
FDA Adverse Event
Injury
·ZIMMER INC.·Product code JWH·June 23, 2011