26 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MICROCUTTER XCHANGE 30 STAPLER, MICROCUTTER XCHANGE 30 BLUE CARTRIDGE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
kitazato IUI Catheter
FDA UDI
KITAZATO CORPORATION·04580303269275·Stylet for 180mm Catheter, model number Type6-v1
Fuji Cervical Plate System
FDA UDI
Altus Spine, LLC·B41711401181·18mm Level 1 Cervical Plate System - Fuji
Accent Buccal Tube
FDA UDI
ORMCO CORPORATION·00889989053722·ORTHOS ACCENT LFM OSGL NDX -10TX18 R
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981201623·Interbody, 11mm x 40mm x 11mm, 8 deg
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319720592·Rochester (Pean) Hemostatic Forceps 5-1/2" (14c...
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981208745·Trial, 11mm x 40mm x 11mm, 8 deg
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981193638·Interbody, 11mm x 40mm x 11mm, 8 deg
VASCULAR SOLUTIONS D-STAT DRY HEMOSTATIC BANDAGE, THE D-STAT RADIAL HEMOSTATIC BAND AND THE D-STAT 2 DRY HEMOSTATIC
FDA 510(k)
FDA Unclassified
·Unknown
STIMTRODE SINGLE USE NERVE STIMULATOR
FDA 510(k)
FDA Class 2
·Anesthesiology
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
FDA Adverse Event
Injury
·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·June 23, 2014
Widex
FDA UDI
Widex A/S·05706069716016·Widex EVOKE E-FP (Tech Black ) 440, Telecoil, V...
Widex
FDA UDI
Widex A/S·05706069923490·WIDEX MOMENT MBB3D 440 (Tech black)
Widex
FDA UDI
Widex A/S·05706069715668·Widex EVOKE E-FA (Tech Black ) 440, Telecoil, V...
Widex
FDA UDI
Widex A/S·05706069884586·WIDEX MOMENT MRR2D (Tech Black ) 440, RC coil, ...
Widex
FDA UDI
Widex A/S·05706069972290·WIDEX MOMENT MBB2 440 (Tech black)
Widex
FDA UDI
Widex A/S·05706069718270·Widex EVOKE E-FM (Tech Black ) 440, RC coil
K-WIRE
FDA Adverse Event
Injury
·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code HWC·December 9, 2016
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
FDA Adverse Event
Injury
·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 25, 2014
MAGEC SPINAL BRACING AND DISTRACTION SYSTEM
FDA Adverse Event
Injury
·ELLIPSE TECHNOLOGIES, INC.·Product code PGN·May 21, 2014