48 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEOSET BVF KIT
FDA 510(k)
FDA Class 2
·Orthopedic
Endo Carry-on Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964150760·Endo Carry-on Procedure Kit contains Intercept ...
MEDRAD® Veris™ 8600 Vital Signs Monitor
FDA UDI
BAYER MEDICAL CARE INC.·00616258009414·"Pediatric Blood Pressure Disposable Cuffs 2-4...
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033167236·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033167205·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033167243·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033167199·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033167212·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033167229·
Intess L
FDA UDI
Kalitec Direct LLC·B07312K0100320·Assembly, Caddie, 30mm Lumbar Implants, Hinged
JEL 15
FDA 510(k)
FDA Class 2
·Dental
DYNA-LOK CLASSIC SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
STREP A RAPID TEST STRIP (THROAT SWAB)
FDA Adverse Event
Death
·ABON BIOPHARM (HANGZHOU) CO., LTD.·Product code GTY·March 25, 2024
ACCU-CHEK ® SPIRIT COMBO
FDA Adverse Event
Malfunction
·ROCHE DIABETES CARE AG·Product code LZG·March 19, 2013
UNKNOWN ZIMMER TIBIAL INSERT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·March 1, 2011
JAWZ
FDA Adverse Event
Malfunction
·ARGON MEDICAL DEVICES, INC.·Product code KNW·February 18, 2008
Upper roller bracket (part number 1088370) for the Gen2 gantry enclosure for the Radixact Treatment Delivery System.
FDA Enforcement
Class II
·Completed·Accuray Incorporated·September 6, 2023
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·July 5, 2013
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·July 5, 2013
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·July 5, 2013