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

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Tranberg CLS Laser Fiber

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

ProLift Trial

FDA UDI
Life Spine, Inc.·00190837088934·

V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER

FDA 510(k)
FDA Class 2 ·Cardiovascular

RINGLOC BI-POLAR ACETABULAR COMPONENT

FDA 510(k)
FDA Class 2 ·Orthopedic

E1 RINGLOC BIPOLAR 28X51MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 31, 2016

RINGLOC HIP SYSTEM ACETABULAR BI-POLAR CUP

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·June 15, 2017

E1 RINGLOC BIPOLAR 28X43MM

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code HBE·June 22, 2016

E1 HI-WALL LINER RINGLOC-X

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·June 2, 2017

RINGLOC BI-POLAR ACETABULAR COMPONENT

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·December 7, 2016

VIRTUOSO DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 7, 2013

GORE INTRODUCER SHEATH WITH SILICONE PINCH VALVE

FDA Adverse Event
Injury ·W.L. GORE & ASSOCIATES·Product code DYB·June 28, 2011

ELECTRO SURGICAL UNIT

FDA Adverse Event
Malfunction ·VALLEY LAB INC.·Product code GEI·September 3, 2008

E1 RINGLOC BIPOLAR 22X40MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 30, 2017

E1 RINGLOC BIPOLAR 28X54MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 26, 2016

E1 RINGLOC BIPOLAR 28X50MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·May 2, 2018

RINGLOC HIP SYSTEM ACETABULAR BIPOLAR CUP

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·January 6, 2017

E1 RINGLOC BIPOLAR 28X53MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 29, 2021

E1 RINGLOC BIPOLAR 28X47MM

FDA Adverse Event
Malfunction ·BIOMET ORTHOPEDICS·Product code JDI·May 3, 2017

RINGLOC BIPOLAR VIT E 28X44MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·February 18, 2025

E1 RINGLOC BIPOLAR 28X51MM

FDA Adverse Event
Malfunction ·ZIMMER BIOMET, INC.·Product code JDI·October 26, 2020