114 results
·
31ms
·
Sources: EU EUDAMED, US FDA
CompleClear Plastic Orthodontic Bracket and Wire Appliance
FDA 510(k)
FDA Class 2
·Dental
Oticon
FDA UDI
Oticon A/S·05707131280879·H16V2, BTE 13 WL 100 SGR
DD base P HI
FDA UDI
Dental Direkt GmbH·EDDIK508301·DD medical polymers (PMMA), made from PMMA, are...
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868344343·
Ophthalmic Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668100103·BARRAQUER SPECULUM SOLID LARGE
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304006843·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197515818·RZ Tebbet Breast Retractor
150x30...
ZODIAC SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
M7/M7T DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BIOMET TOTAL KNEE PROSTHESIS
FDA Adverse Event
Injury
·BIOMET·Product code JWH·March 12, 1997
BIOMET BONE CEMENT R 40X2
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·November 9, 2016
BIOMET BONE CEMENT V
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016
BIOMET BONE CEMENT V
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 1, 2016
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·June 14, 2016
REFOBACIN BONE CEMENT R 2X40G
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·February 2, 2018
OPTIPAC-S KNEE REFOBACIN PLUS BONE CEMNT
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 25, 2016
BIOMET BONE CEMENT 1X40G
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·July 22, 2016
BIOMET BONE CEMENT R 2X40G
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·July 9, 2016
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 23, 2016
OPTIPAC-S 40 REFOBACIN PLUS BONE CEMENT
FDA Adverse Event
Malfunction
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 25, 2016