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

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ALAMO T

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04064984699557·GENUMEDI PSS BLUE SIZE III

Bernafon

FDA UDI
Bernafon AG·05711584052488·JU7 ITCD, WL R BE JUNA 7

PRINCETON

FDA UDI
Princeton Medical Group, Inc.·00810158216709·FORCEPS JEWELER FIG. 3 .3MM TIP 4.75"

ADSON TISSUE FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896076433·ADSON TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLAT...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197053020·DANDY Hemostatic Forceps,1x2 teeth 140mm,...

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197053037·Moynihan delicate artery forceps, cvd. 150mm, 6"

ANGIOSCULPT PTA SCORING BALLOON CATHETER MODEL 2039-XXYY, 2076-XXYY, 2092-XXYY, 2105-XXYY

FDA 510(k)
FDA Class 2 ·Cardiovascular

59% EXTREME H2O (HIOXIFILCON A) SOFT CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

STRATUS CS

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DAP·November 11, 2015

LOGIC FEMORAL PS POR RIGHT SZ 2

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

STRATUS CS

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC - GLASGOW·Product code DAP·November 9, 2015

RESTORE ADVANCED

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 31, 2013

LIFEVEST WCD 3000 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 15, 2011

2250051-2008-00286

FDA Adverse Event
Malfunction ·Product code KSZ·June 12, 2008

BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 24, 2021

SYRINGE 5ML SALINE FILL CHINA SP

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code NGT·October 17, 2023

BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET PRE-ATTACHED HOLDER

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·April 14, 2026

LOGIC CR FEMORAL POR, LEFT, SZ 3.5

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·December 20, 2023