Medical Device Manufacturer · US , Fremont , CA

Optovue, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 2006

Total

Cleared

Denied

Optovue, Inc. has 16 FDA 510(k) cleared ophthalmic devices. Based in Fremont, US.

Last cleared in 2022. Active since 2006.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Optovue, Inc.

16 devices

1-12 of 16

RTVue XR OCT Avanti with AngioVue Software

IVUE WITH NORMATIVE DATABASE

RTVUE CAM WITH CORNEAL POWER UPGRADE

RTVUE MODEL RTVUE 100

K101505 · HLI

Ophthalmic · 106d

Optovue, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) cleared devices by Optovue, Inc.

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