13 results · 29ms · 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.

CoreLink Navigation Instruments

FDA 510(k)
FDA Class 2 ·Neurology

DeBakey Extra-Fine Occlusion Clamp 15mm 17cm curved shanks

FDA UDI
Geister Medizintechnik GmbH·04057034058855·DeBakey Extra-Fine Occlusion Clamp 15mm 1...

DEKA RESEARCH & DEVELOPMENT CORP.

FDA registration
DEKA RESEARCH & DEVELOPMENT CORP.·12 products·🇺🇸 United States

Synapse 3D Cardiac Tools

FDA 510(k)
FDA Class 2 ·Radiology

EX-308 EXCIMER LASER FOR PHOTOTHERAPY TREATMENT OF VITILIGO

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

LINEAR ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 17, 2023

QT SCANNER 2000 MODEL A

FDA Adverse Event
Injury ·QT IMAGING HOLDINGS, INC.·Product code IYO·October 30, 2025

ANALYST DR, DF-4 CONNECTOR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·November 3, 2014

RADIAL JAW 4 BIOPSY FORCEPS

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·August 23, 2011

PELVICOL 2CMM X 7CM 1.0MM

FDA Adverse Event
Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·July 3, 2013

LIFE SCOPE PT

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·December 26, 2023

LIFE SCOPE PT

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·December 8, 2023

Synthes Soft Tissue Retractor Small Extendible Offset blade facilitates easy preparation of the epipereosteal cavity for percutaneous plate insertion.

FDA Enforcement
Class II ·Terminated·Synthes USA HQ, Inc.·November 27, 2013