87 results · 26ms · Sources: EU EUDAMED, US FDA

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ELIA(TM) CARDIOLIPIN IGA IMMUNOASSAY

FDA 510(k)
FDA Class 2 ·Immunology

Bernafon

FDA UDI
Bernafon AG·05711584050040·PC7 CP, VC PS DB PRECISO 7

DVR® CROSSLOCK

FDA UDI
Biomet Orthopedics, LLC·00887868446252·

DVR® CROSSLOCKNARROW PLATE LEFT (HEAD WIDTH X OVERALL LENGTH)

FDA UDI
Biomet Orthopedics, LLC·00880304811799·

DVR® CROSSLOCKNARROW MINI PLATE LEFT (HEAD WIDTH X OVERALL LENGTH)

FDA UDI
Biomet Orthopedics, LLC·00880304811836·

DVR® CROSSLOCK

FDA UDI
Biomet Orthopedics, LLC·00887868446269·

BIOPSY VALVE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MODIFICATION TO COOK ZILVER BILIARY STENT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·March 14, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·August 10, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·February 22, 2018

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code NKB·July 13, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 5, 2019

K-WIRE ATTACHM F/EPD+APD

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWE·October 1, 2014

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE·Product code KDJ·May 29, 2013

ENTRUST AT

FDA Adverse Event
Injury ·MEDTRONIC S.A.·Product code LWS·June 16, 2011

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·July 12, 2019