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

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RESUSCITATION TIMER, MODEL L770-CPR

FDA 510(k)
FDA Class 2 ·Anesthesiology

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496062080·SCOTTISH 70, SIZE M, BLU NAVY, GRADUATED COMPRE...

RN Positioning Cylinder for Solid Abutment 032030

FDA UDI
BIO CONCEPT Co., Ltd.·06947600302209·

N/A

FDA UDI
BIOMET MICROFIXATION, INC·00841036026110·

Kalitec Universal Instruments

FDA UDI
Kalitec Direct LLC·B07301K0620000·Universal Removal Set

SSD-5000 DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

BEHRING COAGULATION SYSTEM, MODEL BCS

FDA 510(k)
FDA Class 2 ·Hematology

iCOR

FDA UDI
TELEFLEX INCORPORATED·09555342303919·FH

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 19, 2011

COLONRING/ COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 19, 2011

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 19, 2011

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 19, 2011

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 19, 2011

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 26, 2011

COLONRING/COMPRESSION ANASTOMOSIS RING (CAR27)

FDA Adverse Event
Injury ·NITI SURGICAL SOLUTIONS LTD.·Product code FZP·August 12, 2011

BABY CONTROL WALL MOUNT INFANT WARMER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code FMT·April 16, 2013

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·September 4, 2014

9600

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 6, 2011

IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.

FDA Enforcement
Class II ·Ongoing·LTS Therapy Systems, LLC·August 6, 2025

IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal patch.

FDA Recall
Open, Classified ·LTS Therapy Systems, LLC·Product code EGJ·May 22, 2025