18 results · 24ms · Sources: EU EUDAMED, US FDA

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OSSIOfiber® Suture Anchor 2.5-3.5 mm

FDA 510(k)
FDA Class 2 ·Orthopedic

Cascadia™ Interbody System

FDA UDI
VB Spine LLC·10888857369993·Trial, Size 12x14x9 mm, 30°

Tokuyama Universal Bond II

FDA 510(k)
FDA Class 2 ·Dental

ABMD Software

FDA 510(k)
FDA Class 2 ·Radiology

ALARIS SYSTEM

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·November 2, 2023

HARMONIC ACE + 7

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 11, 2014

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·July 29, 2011

GYNECARE TVT RETROPUBIC SYSTEM

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·July 23, 2013

BI-METRIC POROUS FMRL 14X150MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·May 1, 2019

M2A-MAGNUM MOD HD SZ 50MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JDI·May 1, 2019

M2A-MAGNUM RECAP CUP 56ODX50ID

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code KWA·May 1, 2019

RATTLER XL CANNULATED INTERFERENCE SCREW

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HWC·January 9, 2018

RATTLER CANNULATED INERFERENCE SCREW

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HWC·January 9, 2018

ACT ARTIC E1 HIP BRG 28X48MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 22, 2019

M2A-MAGNUM PF CUP 54ODX48ID

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·August 22, 2019

MLRY-HD POR FMRL 10X155MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 22, 2019

UNK CUP

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·January 29, 2019

UNKNOWN BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·January 29, 2019