ClearanceBrief
Company ยท US

Oculogica, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (1 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
QEABrain Injury Adjunctive Interpretive Oculomotor Assessment Aid7

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 5, 2026K254086EyeBOX SNAP
Oculogica, Inc.
QEA
Apr 4, 2025K242116EyeBOX EBX-4.1
Oculogica, Inc.
QEA
Dec 22, 2021K212310EyeBOX (Model EBX-4)
Oculogica, Inc.
QEA
Sep 6, 2020K201841EyeBOX
Oculogica, Inc.
QEA
Jul 31, 2019K191183EyeBOX
Oculogica, Inc.
QEA
Dec 28, 2018DEN170091EyeBOX
Oculogica, Inc.
QEA

Latest recalls

DateFirm and productCodeLinked 510(k)
Apr 16, 2019OCULOGICA
EyeBOX Model OCL 02
Terminated
QEANone listed
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