24 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INMODE HAIR REMOVAL (HR) DEVICE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NOVO Health Services, LLC
FDA UDI
NOVO HEALTH SERVICES, LLC·00812564039392·Towel, Flat, 50-Pack NS
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970782·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172971192·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973264·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970751·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970775·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970768·
ENCLOSE ANASTOMOSIS ASSIST DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
PARIETEX PROGRIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
INION OTPS BIOABSOBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·November 18, 2014
INION OTPS BIOABSOBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·May 14, 2015
LOGIC FEMORAL PS POR RIGHT SZ 2
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 10, 2025
INION OTPS BIOABSORBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·March 19, 2015
ENDOPATH** XCEL* BLADELESS TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·May 22, 2013
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Injury
·DEXCOM, INC.·Product code MDS·September 26, 2014
GE LUNAR PRODIGY ADVANCE
FDA Adverse Event
GE HEALTHCARE·Product code KGI·June 9, 2011
LOGIC CR FEMORAL POR, LEFT, SZ 3.5
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·December 11, 2024
HEMOSPHERE FORESIGHT MODULE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code MUD·February 26, 2026
LOGIC CR FEMORAL POR, RIGHT, SZ 3
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·May 14, 2019