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iCam

FDA UDI

Class II (US FDA UDI)

by Optovue, Inc.

Identity

Trade Name
iCam FDA UDI
Generic Name
Ophthalmic fundus camera FDA UDI
Device Name
iCam Camera Head 5 MP FDA UDI
Model / Reference
iCam100 FDA UDI
Description
iCam Camera Head 5 MP FDA UDI

Identifiers

Catalog Number
700-49517-001 FDA UDI
Primary DI / UDI-DI
00858848006278 FDA UDI
510(k) Number
K122572 FDA UDI
FDA Product Code
HKI FDA UDI
GMDN Term
Ophthalmic fundus camera FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1120 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic fundus camera

iCam by Optovue, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic fundus camera.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Optovue, Inc.

Sources (1)

  • FDA UDI 87b662ed-1edd-4e80-917d-2ab58475a58a 36 fields · synced May 30, 2026