31 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PALMAZ GENESIS TRANSHEPATIC BILLARY STENT AND DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890104110·Zirlux Multi-Unit Abutment 2 mmH compatible wit...
PRINCETON
FDA UDI
Princeton Medical Group, Inc.·00810158218451·SCISSOR WESTCOTT OPHTHALMIC BLUNT CURVED FLAT H...
Ovation
FDA UDI
Ortho Development Corporation·00822409121281·Narrow Stem Size 11 STD
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033161401·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033161395·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033161357·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033161289·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033161333·
EZ2C
FDA UDI
FGX INTERNATIONAL INC.·00193033161326·
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0104100·Caddie Lid, Tulip and Domino Connectors
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0134110·Trial, TLIF, 27L OB STR 7Deg, 11mm
CHILI VIDEO, CHILI VIDEOPRO
FDA 510(k)
FDA Class 2
·Radiology
WHOLE PTH (1-84) SPECIFIC IMMUNORADIOMETRIC IRMA DIAGNOSTIC ASSAY KIT, MODEL 3KG056
FDA 510(k)
FDA Class 2
·Clinical Chemistry
010-411-01F
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code CGA·May 23, 1997
010-411-01F SURESTEP
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code CGA·August 21, 1997
010-411-01F UNK
FDA Adverse Event
Injury
·LIFESCAN, INC.·Product code CGA·September 4, 1998
010-411-01F UNK
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·November 5, 1998
010-411-014 UNK
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·November 23, 1998
010-411-01F UNK
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CGA·December 22, 1998