10,000 results
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45ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NuvoMed
FDA UDI
NUVOMED, INC.·00810110301436·DigiEars / LIGHT Bluetooth Neckband Hearing Aid
RETRACTA DETACHABLE EMBOLIZATION COIL
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·October 13, 2020
BYTE DAY ALIGNERS
FDA Adverse Event
Injury
·STRAIGHT SMILE, LLC·Product code NXC·December 13, 2024
CONNECT SFTY SCREW SPIKE NS
FDA Adverse Event
Malfunction
·COVIDIEN·Product code LZH·December 16, 2020
SPEEDBAND SUPERVIEW SUPER 7
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code MND·February 16, 2022
Spoon, Ophthalmic
FDA classification
FDA Class 1
·Spoon, Ophthalmic
AN-B
FDA UDI
AGNES MEDICAL CO., LTD.·08800067700460·Single Use RF Electrode
HLB CO., LTD. HEALTHCARE
FDA registration
HLB CO., LTD. HEALTHCARE·5 products·🇰🇷 South Korea
EPI-HAB PHOENIX, INC
FDA registration
EPI-HAB PHOENIX, INC·1 product·🇺🇸 United States
HLB Life Science CO., LTD
FDA registration
HLB Life Science CO., LTD·2 products·🇰🇷 South Korea
HLB LIFE SCIENCE CO., LTD.
FDA registration
HLB LIFE SCIENCE CO., LTD.·5 products·🇰🇷 South Korea
TI-6AL-7NB URTN
FDA 510(k)
FDA Class 2
·Orthopedic
Versus Catheter (VS110-9NB)
FDA 510(k)
FDA Class 2
·Cardiovascular
H.B. Fuller Medical Adhesive Technologies, LLC
FDA registration
H.B. Fuller Medical Adhesive Technologies, LLC·3 products·🇺🇸 United States
Aileron Posterior Fusion System
FDA UDI
Life Spine, Inc.·00190837030360·Core, Static Aileron, No Bullet, 6mm
Subdural Electrode
FDA UDI
Ad-Tech Medical Instrument Corporation·00841823102935·
Aileron Posterior Fusion System
FDA UDI
Life Spine, Inc.·00190837030544·Core, Static Aileron, No Bullet, 12mm
Aileron Posterior Fusion System
FDA UDI
Life Spine, Inc.·00190837030605·Core, Static Aileron, No Bullet, 14mm
Aileron Posterior Fusion System
FDA UDI
Life Spine, Inc.·00190837030667·Core, Static Aileron, No Bullet, 16mm
Aileron Posterior Fusion System
FDA UDI
Life Spine, Inc.·00190837030728·AILERON Static Posterior Fusion Core, 18mm Slot...