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Visi-Shield for v900L, 2.0x

DermLite LLC · Model V900L-40 · UDI-DI 00850017651302

KYT
6
510(k) clearances
10
Adverse events
1
Recalls
159
Facilities

Description

Visi-Shield for v900L, 2.0x

Recalls

DateFirmReason
2023-03-20DermLite LLCIncorrect labeling; Package labeling contains a different serial number then the serial number on the product labeling.

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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.