30 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RESTORELLE L
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B16741224400·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B1674122440060·
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169606371·SPACER 2122440 O25 23.5MM 12 DEG 14X40
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1224400·12mm H x 24mm W x 40mm L x 0 degrees XLIF
RUSCH
FDA UDI
TELEFLEX INCORPORATED·14026704624376·RUSCH Color Coded Guedel Airway Length 40mm Tra...
BIOMET SMOOTH KNEE STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·September 22, 2019
BIOMET ILOK STEM TIBIAL TRAY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·September 22, 2019
VANGUARD KNEE SYSTEM PS TIBIAL BEARING DCM ARCOM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code HRY·September 22, 2019
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L122440120·12mm H x 24mm W x 40mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X122440120·12mm H x 24mm W x 40mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X12244080·12mm H x 24mm W x 40mm L x 8 degrees XLIF
K2M General Instruments
FDA UDI
VB Spine LLC·10888857554214·Parallel Trial Size 14x30x12 mm
EXPERIENCE®
FDA UDI
Gc Orthodontics America Inc.·D78812244000201·EXCM MBT 022/LR4 -12T 0A
PRESTO BREAST BIOPSY DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
AB DENTAL DEVICES IMPLANTS AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Dental
GMK-PRIMARY FEMUR STD CEMENTED SIZE 4 L
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·December 22, 2020
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 8, 2016
PINNACLE MTL INS NEUT36IDX56OD
FDA Adverse Event
Injury
·8010379 DEPUY INTL., LTD.·Product code KWA·May 21, 2013
BIODESIGN 4-LAYER TISSUE GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH INCORPORATED·Product code FTM·September 18, 2014