28 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INWAVE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Z Liquid HT B4-C 100ml
FDA UDI
ARGEN CORPORATION, THE·D818121820·Dental porcelain/ceramic restoration kit
EXIN
FDA UDI
FOREMOUNT ENTERPRISE CO., LTD.·04719871893401·Standard cushion mask without valve #0
NA
FDA UDI
Smith & Nephew, Inc.·03596010064813·4.0MM PARTIALLY THREADED
...
MONOPTY
FDA UDI
Bard Peripheral Vascular, Inc.·00801741084652·MONOPTY® Disposable Core Biopsy Instrument, 22m...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1218200·12mm H x 18mm W x 20mm L x 0 degrees XLIF
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981216955·Trial, 39mm x 27mm x 18mm, 20 Deg
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981215057·Interbody, 39mm x 27mm x 18mm, 20 Deg
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L121820120·12mm H x 18mm W x 20mm L XLIF Trial 12 degree L...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X12182080·12mm H x 18mm W x 20mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X121820120·12mm H x 18mm W x 20mm L x 12 degrees XLIF
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321218200·
1920898-2018-00829
FDA Adverse Event
Malfunction
·November 2, 2018
NON-STERILE, BLUE & WHITE POWDERED NITRILE EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
AART SILICONE CARVING BLOCK
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
MONOPTY DISPOSABLE CORE BIOPSY INSTRUMENT
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·March 22, 2017
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 21, 2013
TOTALCARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·July 28, 2014
ACCESS 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·May 20, 2011
RING TRANSJUGULAR INTRAHEPATIC ACCESS SET
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·November 15, 2019