24 results · 23ms · Sources: EU EUDAMED, US FDA

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AIM2

FDA 510(k)
FDA Class 2 ·Dental

Darby Dental Supply, LLC

FDA UDI
DARBY DENTAL SUPPLY, LLC·00889813019047·GLOVES LTX PF ALOE&VIT E MED DARBY

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482000366·Symmetry® Chisel, Straight

SureCore Automatic Disposable Biopsy Needle

FDA UDI
Canyon Medical Inc.·06954414640533·Automatic Disposable Biopsy Needle

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361006121·Arena-L, 43X28 Lordotic 12 degrees, 15H

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361006107·Arena-L, 43X28 Lordotic 12 degrees, 11H

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361006138·Arena-L, 43X28 Lordotic 12 degrees, 17H

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361006114·Arena-L, 43X28 Lordotic 12 degrees, 13H

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197499392·Burford Valves, paired 64x65m...

SureCore Automatic Disposable Biopsy Needle

FDA UDI
Canyon Medical Inc.·06954414640830·Automatic Disposable Biopsy Needle

SureCore Automatic Disposable Biopsy Needle

FDA UDI
Canyon Medical Inc.·06954414640380·Automatic Disposable Biopsy Needle

AREX SCRU 2 HEADLESS COMPRESSION SCREWS, MODELS: P2P10, P2P15, P2P20, P2P25, P2P30, P2P35, P2P40, P2P45

FDA 510(k)
FDA Class 2 ·Orthopedic

HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL

FDA 510(k)
FDA Class 2 ·Cardiovascular

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·March 18, 2020

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·September 5, 2019

MEDFUSION

FDA Adverse Event
Malfunction ·ST PAUL·Product code FRN·January 4, 2023

CERTS INLIN VLV W/UNIT BAC CAT

FDA Adverse Event
Injury ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code JXG·February 13, 2024

GYNECARE TVT SECUR SYSTEM

FDA Adverse Event
Injury ·ETHICON SARL·Product code PAH·June 20, 2013

ACCURUS HIGH BRIGHTNESS ILLUMINATOR SYSTEM

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code MPA·July 7, 2011

TERUMO ADVANCED PERFURSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DTQ·September 23, 2008