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Software-Aided Adjunctive Diagnostic Device For Use By Physicians On Lesions Suspicious For Skin Cancer

FDA product code QZS · Class 2 · General, Plastic Surgery

1
Registered devices
11
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

DermaSensor — Dermasensor, Inc.

Recent recalls

DateFirmReason
2025-10-13DERMASENSOR INCPotential for device to not meet specifications resulting in incorrect results or delay of referral for patients.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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