23 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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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