9 results
·
16ms
·
Sources: EU EUDAMED, US FDA
DATA REDUCTION SYSTEM, DP-3000
FDA 510(k)
FDA Class 1
·Clinical Chemistry
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515200937·Glenoid Perforation Fcps, light angle, 6 3/4"
ENDOCERVICAL ELECTRODE # 2
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Parcus SLiK Fix Screw
FDA 510(k)
FDA Class 2
·Orthopedic
STYLE 20 SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·July 29, 2025
STYLE 20 SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·August 4, 2025
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·April 24, 2014
LIGACLIP** ENDOSCOPIC CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 3, 2012
BIO-MODULAR SHOULDER 44 X 17 MM OFFSET HEAD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·July 27, 2010