24 results · 21ms · Sources: EU EUDAMED, 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