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Strabismus Detection Device

FDA product code PMW · Class 2 · Ophthalmic

1
Registered devices
9
Adverse events
1
Recalls
1
510(k) clearances

Devices with this code

Blinq — REBISCAN, INC.

Recent 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

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

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