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Vortex Surgical Inc.

FDA UDI

Class I (US FDA UDI)

by Vortex Surgical, Inc.

Identity

Trade Name
Vortex Surgical Inc. FDA UDI
Generic Name
Scleral marker, single-use FDA UDI
Device Name
Lindsell Sutured IOL Marker FDA UDI
Model / Reference
VS0390 FDA UDI
Description
Lindsell Sutured IOL Marker FDA UDI

Identifiers

Primary DI / UDI-DI
00810123483662 FDA UDI
FDA Product Code
HMQ FDA UDI
GMDN Term
Scleral marker, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4570 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Scleral marker, single-use

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

Similar devices

Also classified as Scleral marker, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 70c7f1c7-7349-481a-907a-efde6d595add 33 fields · synced May 30, 2026