38 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ORTHOSCAN MOBILE DI MINI C-ARM
FDA 510(k)
FDA Class 2
·Radiology
ScrewPlant® Implant
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307105206·3.7mmD x 8mmL, 3.7mmD Platform
BIO-MODULAR SHOULDER SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304204522·
GLOBAL ADVANTAGE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295007098·GLOBAL ADVANTAGE REVISION STEM SIZE 8 200mm
GLOBAL ADVANTAGE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295007104·GLOBAL ADVANTAGE POROCOAT STANDARD STEM SIZE 8 ...
GLOBAL ADVANTAGE
FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295007081·GLOBAL ADVANTAGE STANDARD STEM SIZE 8 133mm
ML24000 UVA-1 PHOTOTHERAPY UNIT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
REFERENCE CHECK, CATALOG NUMBER-RCN-10
FDA 510(k)
FDA Class 2
·Hematology
REFERENCELLS
FDA Adverse Event
Malfunction
·IMMUCOR·Product code KSZ·September 4, 2009
REFERENCELLS
FDA Adverse Event
Malfunction
·IMMUCOR·Product code KSZ·September 4, 2009
ARCHITECT HAVAB-IGG
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·May 8, 2026
ARCHITECT HAVAB-IGG
FDA Adverse Event
Malfunction
·ABBOTT GMBH·Product code LOL·April 3, 2026
NITE PROTECTOR
FDA Adverse Event
Malfunction
·RANIR LLC·Product code OBR·May 1, 2014
TRIFECTA STENTED TISSUE VALVE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL BRASIL LTDA.·Product code LWR·May 10, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·June 2, 2011
UNKNOWN GLENOID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 4, 2017
BIO-MOD HUM HEAD 48DIAX19MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWT·February 21, 2018
MD HYBRID GLENOID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·February 21, 2018
PT HYBRID GLEN POST
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·February 21, 2018
BIO-MOD HUM HEAD 48DIAX19MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 4, 2017