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Lipiview Ii Ocular Surface Interferomete

FDA UDI

Class II (US FDA UDI)

by Tearscience, Inc.

Identity

Trade Name
LIPIVIEW II OCULAR SURFACE INTERFEROMETE FDA UDI
Generic Name
Meibomian gland camera/ophthalmic interferometer FDA UDI
Device Name
ASSEMBLY PKGD LIPIVIEW-2 - US FDA UDI
Model / Reference
LVI-2000 FDA UDI
Description
ASSEMBLY PKGD LIPIVIEW-2 - US FDA UDI

Identifiers

Catalog Number
100100 FDA UDI
Primary DI / UDI-DI
00859623006612 FDA UDI
FDA Product Code
HKI FDA UDI
HJO FDA UDI
GMDN Term
Meibomian gland camera/ophthalmic interferometer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1120 FDA UDI
886.1850 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: Meibomian gland camera/ophthalmic interferometer

Lipiview Ii Ocular Surface Interferomete by Tearscience, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Meibomian gland camera/ophthalmic interferometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tearscience, Inc.

Sources (1)

  • FDA UDI 8480b5e2-ece7-4e09-84dd-77df689ff977 36 fields · synced Jun 1, 2026