17 results · 21ms · Sources: EU EUDAMED, US FDA

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TYTAN REUTER BOBBIN VENT TUBE

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

Tranquil-C™

FDA UDI
NEXUS SPINE, L.L.C.·B6788223760·Cervical Rasp + DS 5x14x12 Flat

Lianfa Safety Lancet (Five Models: NPA, PA, PA2, TPA, and APA)

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

PMT TRUSCAN SURFACE ELECTRODE

FDA 510(k)
FDA Class 2 ·Neurology

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·August 12, 2020

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·May 9, 2024

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·January 14, 2016

MECTALIF POSTERIOR (TI PEEK) POSTERIOR INTERBODY FUSION DEVICE PEEK/TI

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MAX·July 18, 2022

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 20, 2014

RESTORE ULTRA

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·November 7, 2012

ULTRACISION HARMONIC SCALPEL CURVED SHEARS (LCS) - PISTOL GRIP 36 CM - 15 MM ACT

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GEI·August 17, 2007

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·April 11, 2021

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·May 22, 2020

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·June 24, 2019

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·September 11, 2019

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·October 3, 2017

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·May 17, 2018