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Visionix

FDA UDI

Class II (US FDA UDI)

by Luneau Technology Operations

Identity

Trade Name
VISIONIX FDA UDI
Generic Name
Ophthalmic examination slit lamp FDA UDI
Device Name
ophthalmic slit lamp FDA UDI
Model / Reference
VX80 - 5x para FDA UDI
Description
ophthalmic slit lamp FDA UDI

Identifiers

Primary DI / UDI-DI
03664188000831 FDA UDI
510(k) Number
K992836 FDA UDI
FDA Product Code
HJO FDA UDI
GMDN Term
Ophthalmic examination slit lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Ophthalmic examination slit lamp

Visionix by Luneau Technology Operations — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic examination slit lamp.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI da7a5d58-cfb6-4111-9557-f124a2b69940 34 fields · synced May 31, 2026