30 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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T2 HUMERAL NAIL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
MYELO-NATE
FDA UDI
UTAH MEDICAL PRODUCTS, INC.·H67140115290·MYELONATE NEEDLE (1.5") 22GA
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040010525·Zirlux 16+ D3 100X18
Truliant
FDA UDI
Exactech, Inc.·10885862653277·Special Universal Baseplate Tibial Trial, Size 2
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291948·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291962·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291924·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291931·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291979·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291955·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033292006·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291986·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291993·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0115200·Needle, Bevel Stylet, Stainless Steel, Disposable
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033291917·
RESTORE ADVANCED
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 23, 2013
POLYMER COATED, POWDER-FREE LATEX EXAMINATION GLOVE WITH PROTEIN LABELLING CLAIM, CONTAINS 50 MICROGRAMS OR LESS OF TOTA
FDA 510(k)
FDA Class 1
·General Hospital
TITANIUM CEMENT RESTRICTOR MATERIAL PLDLA
FDA 510(k)
FDA Class 2
·Orthopedic
RESTORE ADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·January 23, 2013
INSTAHEET INSTANT HOT COMPRESS
FDA Adverse Event
Malfunction
·NORTECH LABORATORIES, INC.·Product code IMD·July 15, 2015