15 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DERMASENSOR INC
FDA registration
DERMASENSOR INC·1 product·🇺🇸 United States
DermaSensor
FDA UDI
Dermasensor, Inc.·00850017786004·
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·December 29, 2025
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·December 30, 2025
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·January 27, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·January 27, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·February 2, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·January 27, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·January 27, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·January 27, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·January 27, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·February 9, 2026
DERMASENSOR
FDA Adverse Event
Malfunction
·DERMASENSOR INC·Product code QZS·January 27, 2026
DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer
FDA Recall
Open, Classified
·DERMASENSOR INC·Product code QZS·October 13, 2025
DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer
FDA Enforcement
Class II
·Ongoing·DERMASENSOR INC·December 3, 2025