40 results · 22ms · Sources: EU EUDAMED, US FDA

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FDA 510(k)
FDA Class 2 ·Cardiovascular

JOBST Bella Lite

FDA UDI
BSN MEDICAL, INC.·00035664013394·BELLA LITE 20-30 MM HG ARMSLEEVE LARGE-LONG BRO...

Clean-Bor Tube 2"ID x 39"

FDA UDI
Vacumed·00850644007862·Clean-Bor Tube

Sklar®

FDA UDI
SKLAR CORPORATION·10649111313608·POSILOCK INSTR STRING 18 X 2.5

Astra Vr

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436111294·ASTRA VR Endovaginal/Endorectal Probe Reprocessor

Indus

FDA UDI
SPINEFRONTIER, INC.·00190361035510·Indus Invue MAX Symmetrical ACP, 2 Level, 39mm

Clean-Bor Tube 2"ID x 39"

FDA UDI
Vacumed·00850644007879·Clean-Bor Tube

OMNILINK ELITE PERIPHERAL STENT SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR·Product code NIO·July 22, 2020

QUEST EXERCISE STRESS SYSTEM, MODEL CONFIGURATION 14

FDA 510(k)
FDA Class 2 ·Cardiovascular

MRI FASTSYSTEM RETRACTOR SYSTEM

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

AVANTAGE INLAY SIZE 50/28

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code LPH·December 15, 2016

UNKNOWN BIOMET AVANTAGE INSERT

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017

AVANTAGE E1 INSERT DIA28 S56

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·July 21, 2016

UNKNOWN BIOMET AVANTAGE INSERT

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·February 16, 2017

G7 BISPHERICAL SHELL 50D

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code LPH·December 15, 2025

AVANTAGE INSERT

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

AML SM STATURE 15.0MM

FDA Adverse Event
Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·May 9, 2013

NATURALYTE

FDA Adverse Event
Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

OT ULTRALINK METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 24, 2011

AVANTAGE UHMWPE INSERT

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code LPH·March 29, 2017