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Blinq

REBISCAN, INC. · Model 1 · UDI-DI 00864816000421

PMW Prescription
1
510(k) clearances
9
Adverse events
1
Recalls
2
Facilities

Description

Blinq Pediatric Vision Scanner

Recalls

DateFirmReason
2022-10-03Rebiscan, Inc.Unable to charge the battery pack- battery packs will allow the batteries to be charged if the voltage of any cell is below 2.5V. When this occurs, the battery pack will not accept

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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.