32 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0140020·Driver Shaft, T30 No Taper, Final Cap Driver
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07310K0140020·Driver Shaft, T30 Final Cap, MIS
ALL SILICONE SUPRA-PUBIA CATHETER, MODELS 4880/4890
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ADVANCE®
FDA UDI
Microport Orthopedics Inc.·M684K00140021·
n/a
FDA UDI
Ortho Development Corporation·00822409072941·Neck Trial Standard Size 4-6
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033547649·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033547595·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033547618·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033547601·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033547656·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033547632·
UNBRANDED
FDA UDI
FGX INTERNATIONAL INC.·00193033547625·
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100020·Tap, 4.5mm Cann, Quarter Square
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0140000·Counter Torque, Standard and Extended Tab
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0100020·Caddie, 1-3 Level Plates
IMMULITE CK-MB, MODEL LKMB1 (100 TESTS), LKMB5 (500 TESTS); IMMULITE 2000 CK-MB, MODEL L2KMB2 (200 TESTS), L2KMB6 (600)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CONTOUR POLARIS URETERAL STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
POLARIS ULTRA
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FAD·June 27, 2019
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
TENDRIL SDX
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·March 10, 2011