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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SURGIVISION MR COMPATIBLE VENTRICULAR CANNULA

FDA 510(k)
FDA Class 1 ·Neurology

EVOTECH™

FDA UDI
ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037000333·Adapter - Water/Air

Huggin

FDA UDI
IPB·00810053770757·Light Body Fast Set Orange, 4 Pack

Tasso+ Convenience Kit

FDA UDI
Tasso Inc.·00860006434526·Tasso+ allows self-collection of a capillary bl...

Dynamic Axial Fixator

FDA UDI
ORTHOFIX SRL·18032568867664·CALIBRATED DRILL BIT D. 4.8 MM L.180 MM

ILIZAROV SYSTEMS

FDA UDI
MEDICALPLASTIC SRL·28033201846890·1,5 MM DIA 300 MM LENGTH ST. STEEL ILIZAROV WIR...

ILIZAROV

FDA UDI
Smith & Nephew, Inc.·23596010031192·WIRE BAYONET POINT CORTICAL 1.5MM ...

REPICCI II RESURFACING KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304184800·

ILIZAROV SYSTEMS

FDA UDI
MEDICALPLASTIC SRL·28033201841710·1,5 MM DIA 300 MM LENGTH ST. STEEL ILIZAROV WIR...

Dynamic Axial Fixator

FDA UDI
ORTHOFIX SRL·18032937169672·CALIBRATED DRILL BIT D.4,8 MM L.190 MM TIN COAT...

GSP NEONATALGALT KIT, MODEL 3303-001U

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

NIAGARA® Lateral Access System

FDA UDI
VB Spine LLC·10888857519923·Blade Holder

NA

FDA UDI
STRYKER CORPORATION·07613327173444·CROSSCUT SUTURE CUTTER

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197202411·RZ Double Clamp, Vein 8mm, 0...

ONE TOUCH BASIC

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·May 10, 2002

CAPI 3 IMMUNOTYPING

FDA Adverse Event
Malfunction ·SEBIA·Product code CFF·September 16, 2021

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 29, 2025

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·September 10, 2019

ARCHITECT C4000 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·May 4, 2015