36 results
·
22ms
·
Sources: EU EUDAMED, US FDA
SYNVITRO CUMULASE (HYALURONIDASE MEDIUM)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Y060699 Wrist Splint
Device
EU MDR
·
Eu Md Class 1
·Welsheng Corp.·On the market
TSRH SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
VERAVIEWEPOCS PANORAMIC/CEPHALOMETRIC X-RAY UNIT WITH CEPHALOMETRIC
FDA 510(k)
FDA Class 2
·Dental
TESS HUM INSERT TH 6 DIA36 S1
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code KWS·March 7, 2017
TESS HUMERAL INSERT TH 8 DIA36 S0
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017
TESS HUMERAL REVERSED INLAY 036 S1 12MM
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·February 9, 2017
TESS HUMERAL INSERT TH 6 DIA36 S0
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017
CUSTOM REVERSE HUMERAL LINER
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·February 27, 2017
TESS GLEN BASEPLATE S0
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·May 25, 2016
AMPLATZER SEPTAL OCCLUDER
FDA Adverse Event
Injury
·AGA MEDICAL CORPORATION·Product code MLV·September 30, 2019
AMPLATZER SEPTAL OCCLUDER
FDA Adverse Event
Injury
·AGA MEDICAL CORPORATION·Product code MLV·September 30, 2019
TESS HUMERAL REVERSE COROLLA S0
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·November 18, 2016
UNKNOWN TESS GLENOID COMPONENT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·July 7, 2017
TESS HUM INSERT TH 6 DIA36 S0
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code KWS·May 10, 2017
UNKNOWN TESS HUMERAL INSERT
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code KWS·June 1, 2017
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·March 29, 2013
LARGE FRAG SCREWDRIVER
FDA Adverse Event
Injury
·SYNTHES, INC.·Product code HXX·June 10, 2008
UNKNOWN DEPUY LCS FEMORAL COMPONENT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·April 6, 2011
COMPR 12MM IM HMRL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·April 1, 2019