17 results · 21ms · Sources: EU EUDAMED, US FDA

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PowerMidline Catheter

FDA 510(k)
FDA Class 2 ·General Hospital

Clinician's Choice® Low Viscosity Tubes & Plugs

FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002257·Dental material injection cannula, single-use

Mouthpiece, Disposable, 1 1/16" OD, 3.25" L

FDA UDI
A-M SYSTEMS, LLC·00817081023879·Mouthpiece, Disposable, 1 1/16" OD, 3.25" L

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702616279·ELVAREX 2/KNEE HIGH/SLANT-OPEN TOE-ELEPHANTIASI...

II Ring Retractor

FDA UDI
Automated Medical Products Corp.·00810118342585·Richardson Retractor 1" x 1 1/2"

PAJUNKS STIMULONG TSUI-METHOD SET

FDA 510(k)
FDA Class 2 ·Anesthesiology

HEITER 3000 HYPERTHERMIC PERFUSION SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2025

PAINSMART IOD

FDA Adverse Event
Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 15, 2011

CONSULTA CRT-D

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·October 10, 2014

VANGUARD XP-XP MEDIAL BEARING TIBIAL TRAY E1 ANTIOXIDANT INFUSED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·July 2, 2018

VANGUARD XP-XP LATERAL BEARING TIBIAL TRAY E1 ANTIOXIDANT INFUSED

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 2, 2018

VANGUARD XP TIBIAL LOCKING BAR

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·July 2, 2018

VANGUARD XP FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MBH·July 2, 2018

BIOMET SERIES A STANDARD PATELLA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 2, 2018

XP-XP Tibial Tray - Interlok 65 mm Item # 195752

FDA Enforcement
Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019