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

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SIMPLY SLICK PERSONAL LUBRICATING LOTION

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04064984699564·GENUMEDI PSS BLUE, SIZE IV

CoRoent

FDA UDI
Nuvasive, Inc.·00887517565686·CoRoent Ant TLIF PEEK, 14x10x30mm 4°

PRINCETON

FDA UDI
Princeton Medical Group, Inc.·00810158217201·FORCEPS JEWELER FIG. 3C .5MM TIP 4.25"

ADSON TISSUE FORCEPS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896023482·ADSON TISSUE FORCEPS WITH TUNGSTEN CARBIDE PLAT...

PHILIPS INTELLIVUE PATIENT MONITOR, MODELS MP40 & MP50

FDA 510(k)
FDA Class 2 ·Cardiovascular

ST AIA PACK HBA1C

FDA 510(k)
FDA Class 2 ·Hematology

HIGH FREQUENCY VENTED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·December 4, 2014

LOGIC FEMORAL PS POR RIGHT SZ 2

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

GMK PS FEMUR CEMENTED SIZE 2 LEFT

FDA Adverse Event
MEDACTA INTL SA·Product code JWH·May 24, 2013

EEA 28MM SINGLE-USE STAPLER

FDA Adverse Event
Injury ·USSC PUERTO RICO·Product code GDW·June 15, 2011

UNKNOWN_RECONSTRUCTIVE_PRODUCT

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·October 3, 2014

LOGIC CR FEMORAL POR, LEFT, SZ 3.5

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

ALARIS SYSTEM

FDA Adverse Event
Injury ·CAREFUSION SD·Product code FRN·May 13, 2022

ALARIS SYRINGE PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·December 23, 2020

VACUTAINER ULTRATOUCH

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code FPA·March 23, 2026

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·March 29, 2022

CATHETER MOUNT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZO·December 29, 2014

INFANT DUAL HEATED EVAQUA2 BREATHING CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·December 4, 2014

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 26, 2023