9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
STRUNG DENTAL ROLLS
FDA 510(k)
FDA Class 1
·Dental
PRONTO LOW PROFILE (LP) EXTRACTION CATHETER, MODEL 5010
FDA 510(k)
FDA Class 2
·Cardiovascular
PORT-X IV
FDA 510(k)
FDA Class 2
·Dental
M2A MAGNUM SYSTEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·March 17, 2017
M2A-MAGNUM MOD HD SZ 42MM 42MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·October 30, 2019
M2A-MAGNUM PF CUP 48ODX42ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·October 30, 2019
EMAX 2 PLUS MOTOR
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 13, 2014
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·October 14, 2010
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - GUANGZHOU·Product code KDI·December 13, 2012