Vortex Surgical Inc.

FDA UDI

Class II (US FDA UDI)

by Vortex Surgical, Inc.

Identity

Trade Name: Vortex Surgical Inc. FDA UDI
Generic Name: Ophthalmic laser system beam guide FDA UDI
Device Name: 25ga Illuminated Curved Laser Probe - Multiport FDA UDI
Model / Reference: VS0125.25 FDA UDI
Description: 25ga Illuminated Curved Laser Probe - Multiport FDA UDI

Identifiers

Primary DI / UDI-DI: 00810123483648 FDA UDI
FDA Product Code: HQB FDA UDI
MPA FDA UDI
GMDN Term: Ophthalmic laser system beam guide FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 886.4690 FDA UDI
876.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Ophthalmic laser system beam guide

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

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Also classified as Ophthalmic laser system beam guide.

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23-27G BriteLight™ Angled 45° EndoProbe® Box of 6 — Iridex Corporation · Class II
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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: Vortex Surgical, Inc.

Sources (1)

FDA UDI 924b5108-9d89-44f3-bc79-eed220403c9c 33 fields · synced May 30, 2026