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

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PALS NEONATAL PEDIATRIC ECG ELECTRODE, MODELS PN100, PN200

FDA 510(k)
FDA Class 2 ·Cardiovascular

ACE

FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950016563·CURETTE BONE MILLER #12 D/E 7" 18CM TIP SIZE AP...

intellijoint HIP®

FDA UDI
Intellijoint Surgical Inc·00628184002063·V-Block, G2

SCHWERT

FDA UDI
A. Schweickhardt GmbH & Co. KG·E89620002060·Needle holders 18cm curved diamond coated...

SILVERVENT

FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948000214·SILVERVENT 2 IC, SIZE 6

PRCT2

FDA UDI
FX SOLUTIONS·03701037301869·PRCT2, DIAPHYSEAL PLATE TA6V 6 HOLES

Matrix Wearable

FDA UDI
GLOBAL INSTRUMENTATION, LLC·00815187020112·M5 Patient Cable Cradle

BONE SCREWS DIA. 6.5 X H. 35 MM

FDA Adverse Event
Malfunction ·LIMACORPORATE SPA·Product code LPH·March 24, 2022

FlowLogic Agile

FDA UDI
SONENDO, INC.·00810209420161·FlowLogic Agile Shaping File 20/.06, 21mm

IMMULITE PHENYTOIN, IMMULITE 2000 PHENYTOIN, CATALOG # LKPN1, LKPN5 & L2KPN2, L2KPN6

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

APPLE MEDICAL ONE-TOUCH UTERINE SAMPLER

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

FEMORAL MODULAR HEAD - L Ø36MM

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code LPH·August 9, 2022

CARDIOSAVE HYBRID W/ E/F PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·January 15, 2025

5.0CM SHORT ATTACHMENT

FDA Adverse Event
Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·February 14, 2013

SELOX ST 60

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·February 18, 2011

DISPOSABLE PURSTRING 65 INSTRUMENT

FDA Adverse Event
Injury ·PONCE - USS·Product code GAG·February 19, 2008

3MM ELASTIC STAYS 8/PK

FDA Adverse Event
Malfunction ·COOPERSURGICAL, INC.·Product code GAD·September 27, 2024

AIA-900

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code KHO·January 28, 2019

SMR CEMENTLESS FINNED STEM

FDA Adverse Event
Injury ·LIMACORPORATE S.P.A.·Product code HSD·March 11, 2022

Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A, View Station Software Kit 0020-00-0206-16A, Work Station Software Kit 0020-00-0207-16A, Software Kit Upgrade TECH-00-910. The Panaroma Patient Monitoring Network is intended for use in a fixed location in the healthcare facility setting as a central viewing station. It is not intended to be directly connected to patient at any time or installed in a patient's vicinity.

FDA Recall
Terminated ·Mindray DS USA, Inc. dba Mindray North America·Product code MHX·December 15, 2015