134 results · 23ms · Sources: EU EUDAMED, US FDA

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NICOLET WIRELESS EEG

FDA 510(k)
FDA Class 2 ·Neurology

PMT CORPORATION - STEREOTACTIC

FDA UDI
PMT CORPORATION·00650551149330·STERILIZATION TRAY FOR VERTEK SEEG KIT FOR 2.4M...

PIN CUTTER

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896099777·PIN CUTTER DOUBLE ACTION TUNGSTEN CARBIDE BLADE...

NexxZr™ / W-98-25-UT-C400-ML

FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271139580·

Orthopaedic Surgical Instruments

FDA UDI
CITIEFFE SRL·08056711921365·

Taperloc Complete Primary Femoral

FDA UDI
Biomet Orthopedics, LLC·00880304491816·

FLIERINGA SCLERAL FIXATION RING

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896088399·FLIERINGA SCLERAL FIXATION RING

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197202527·Clamp Applying Forceps Fig. 1, 2 straig...

RHODIA HYDROPHILIC DENTAL IMPRESSION MATERIAL

FDA 510(k)
FDA Class 2 ·Dental

DENTLIGHT ORAL EXAM LIGHT KIT

FDA 510(k)
FDA Class 2 ·Dental

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 15, 2022

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·May 16, 2023

ONE TOUCH ULTRA

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·June 4, 2002

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·March 23, 2023

T:SLIM G5 SYSTEM

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OYC·October 12, 2018

GMK REVISION TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 15, 2026

TAPERLOC COMPLETE PRIMARY FEMORAL

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS, LLC·Product code KWL·August 10, 2021

TPRLC 133 FP TYPE1 PPS SO 4.0

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code KWY·June 10, 2019

TPRLC 133 T1 PPS HO 16X152MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code KWY·June 7, 2019

TPRLC 133 FP TYPE1 PPS SO 8.0

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code KWY·June 7, 2019