25 results · 21ms · Sources: EU EUDAMED, US FDA

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ROCHE DIAGNOSTICS CK-MB

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

TruForm

FDA UDI
Rmo, Inc.·00885797099709·MX MLR BDS R/L SE ASIA ASST100

GEN4 INTERACTIVE

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828117494·GEN4 INTERACTIVE

SCANLAN® Titanium Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159008586·Micro Forceps, Round Handle, str DD platform ti...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450482872·

SCANLAN® Titanium Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159018936·TITANIUM MICRO FORCEPS ROUND HANDLE STRT PLTFM ...

SCANLAN® Titanium Neuro Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159012002·Micro Suture Tying Fcp, RH, Gerald type taper, ...

SCANLAN® Titanium Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159008593·Micro Forceps, Round Handle, str DD platform ti...

SCANLAN® Titanium Neuro Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159036268·Micro Suture Tying Fcp, RH, Gerald type taper, ...

SCANLAN® Titanium Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159008609·Micro Forceps, Round Handle, str DD platform ti...

SCANLAN® Titanium Forceps

FDA UDI
SCANLAN INTERNATIONAL INC·00846159008616·Micro Forceps, Round Handle, str DD platform ti...

INSET GUARD

FDA Adverse Event
Malfunction ·UNOMEDICAL A/S·Product code FPA·March 30, 2026

VEINLASE, MODEL E50-K8-B5, SPECTRUM K8, MODEL E50-K8-B9

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

EBI XFIX DFS METAPHYSEAL CORRECTION SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

ALLOFT-S ALLOCLASSIC SHL 52/II

FDA Adverse Event
Malfunction ·ZIMMER GMBH·Product code JDI·March 12, 2019

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013

CLARION

FDA Adverse Event
Malfunction ·ADVANCED BIONICS, LLC·Product code MCM·February 14, 2011

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·August 12, 2014

ALLOFIT-S ALLOCLASSIC, SHELL WITH POLAR SCREW PLUG, UNCEMENTED, 52/II

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code LZO·September 27, 2018

INFUSOMAT®

FDA Adverse Event
Malfunction ·B BRAUN MELSUNGEN AG·Product code FRN·November 15, 2023