Liquid Optics Interface

FDA UDI

Class II (US FDA UDI)

by Johnson & Johnson Surgical Vision, Inc.

Identity

Trade Name: LIQUID OPTICS INTERFACE FDA UDI
Generic Name: Ophthalmic laser system beam guide FDA UDI
Device Name: DAILY ALIGNMENT VERIF INTERFACE,GEN2 LOI FDA UDI
Model / Reference: 0180-2010 FDA UDI
Description: DAILY ALIGNMENT VERIF INTERFACE,GEN2 LOI FDA UDI

Identifiers

Catalog Number: 0180-2010 FDA UDI
Primary DI / UDI-DI: 05050474651487 FDA UDI
FDA Product Code: OOE FDA UDI
GMDN Term: Ophthalmic laser system beam guide FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.4390 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Ophthalmic laser system beam guide

Liquid Optics Interface by Johnson & Johnson Surgical Vision, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Johnson & Johnson Surgical Vision, Inc.

Sources (1)

FDA UDI 629f00b8-c285-49a2-a3b2-927029209e8e 36 fields · synced Jun 9, 2026