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Optain

FDA UDI

Class II (US FDA UDI)

by Optain Health, Inc.

Identity

Trade Name
Optain FDA UDI
Generic Name
Ophthalmic fundus camera FDA UDI
Device Name
The Resolve Fundus Camera is an automatic eye-fundus camera intended for taking digital images of a human retina with or without the use of a mydriatic agent. It is intended for use as an aid to clinicians in the evaluation and diagnosis of ocular health. FDA UDI
Model / Reference
Resolve Fundus Camera FDA UDI
Description
The Resolve Fundus Camera is an automatic eye-fundus camera intended for taking digital images of a human retina with or without the use of a mydriatic agent. It is intended for use as an aid to clinicians in the evaluation and diagnosis of ocular health. FDA UDI

Identifiers

Primary DI / UDI-DI
00860014304507 FDA UDI
510(k) Number
K250683 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
MRI Safety
MR Unsafe FDA UDI

Category: Ophthalmic fundus camera

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

Similar devices

Also classified as Ophthalmic fundus camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Optain Health, Inc.

Sources (1)

  • FDA UDI c048d5ec-e42d-4ca4-9aef-8543c80a9d11 34 fields · synced May 30, 2026