23 results · 21ms · 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.

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM, TRANSLATIONAL PLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWQ·May 10, 2018

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·February 10, 2025

28 Aero Incubator Transporter

FDA UDI
FERNO-WASHINGTON, INC.·00190790002190·28 Aero IT

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496063100·SOCKS FOR YOU BAMBOO MUSIC, SIZE L, BLU NAVY, G...

Clinician's Choice® #1 Instrument

FDA UDI
CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172001113·Dental restorative material applicator

Sklar®

FDA UDI
SKLAR CORPORATION·40649111180935·SURG BLADES SS STER #10 100'S

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702395600·ELVAREX FORTE 3/KNEE HIGH/PROFILE-OPEN TOE-ELEP...

FORE-SIGHT ELITE®

FDA UDI
CAS MEDICAL SYSTEMS, INC.·10609538631006·Tissue Oximeter Preamp

MetaSystems Probes

FDA UDI
MetaSystems Probes GmbH·04251315818231·XL 4q12, Translocation/Deletion Probe

WALLGRAFT TRACHEOBRONCHIAL ENDOPROSTHESIS AND UNISTEP DELIVERY SYSTEM

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

PROPOXYPHENE

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523107070·Pre Lordosed Rod 6.0mm diameter 100mm length Ti...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523107902·Pre Lordosed Rod 6.0mm diameter 100mm CoCr

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523107667·Pre Lordosed Rod 6.0mm diameter 100mm length CP...

Widex

FDA UDI
Widex A/S·05706069633221·Compass V5.9.2 CD-ROM

PLEXOLONG NANOLINE MEIER

FDA Adverse Event
Other ·PAJUNK GMBH MEDIZINTECHNOLOGIE·Product code CAZ·April 11, 2013

AFFINITY BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·March 16, 2011

LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

FDA Adverse Event
Malfunction ·FRESENIUS REYNOSA MANUFACTURING·Product code FKX·August 8, 2014