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DermaSensor

Dermasensor, Inc. · Model 10101 · UDI-DI 00850017786004

QZS
1
510(k) clearances
11
Adverse events
1
Recalls
2
Facilities

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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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.