23 results · 28ms · Sources: EU EUDAMED, US FDA

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MADgic Laryngo-Tracheal Mucosal Atomization Device

FDA 510(k)
FDA Class 2 ·Anesthesiology

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776189747·BIOPSY CUP FORCEPS

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100318·ALPHONSO INFANT SPECULUM

NOVOFINE 32G TIP

FDA 510(k)
FDA Class 2 ·General Hospital

PANTHER GROUP OF SURGICAL INCLUDES: OANTHER CIRCULAR STAPLER; PANTHER HEMORRHOIDAL CIRCULAR STAPLER; PANTHER LINEAR STAP

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

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·June 16, 2025

COGNIS

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·July 7, 2011

CAPSUREFIX NOVUS

FDA Adverse Event
Malfunction ·MPRI·Product code DTB·June 8, 2013

ELLIPSE ST DR, DF-4 CONNECTOR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·October 8, 2014

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

DYB INTRODUCER, CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code DYB·November 12, 2025

FLEXOR SHUTTLE SELECT GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

OSS POLYETHYLENE LOCKING PIN

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018

OSS POLYETHYLENE TIBIAL BUSHING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018

OSS TIBIAL POLYETHYLENE BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018

OSS REINFORCED YOKE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 26, 2018

OSS LONG TIBIAL PLATE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018

OSS PROXIMAL TIBIAL POROUS COATED STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 23, 2018

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 15, 2020