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Clareon Vivity Toric Extended Vision UV Absorbing IOLs with the AutonoMe

FDA UDI

Class III (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
Clareon Vivity Toric Extended Vision UV Absorbing IOLs with the AutonoMe FDA UDI
Generic Name
Posterior-chamber intraocular lens, pseudophakic FDA UDI
Device Name
CLAREON UVA VIVITY TORIC AUTONOME FDA UDI
Model / Reference
CCAET4 FDA UDI
Description
CLAREON UVA VIVITY TORIC AUTONOME FDA UDI

Identifiers

Catalog Number
CCAET4.080 FDA UDI
Primary DI / UDI-DI
00380658408022 FDA UDI
FDA Product Code
POE FDA UDI
GMDN Term
Posterior-chamber intraocular lens, pseudophakic FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
886.3600 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Posterior-chamber intraocular lens, pseudophakic

Clareon Vivity Toric Extended Vision UV Absorbing IOLs with the AutonoMe by Alcon Laboratories, Inc. — Class III — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Posterior-chamber intraocular lens, pseudophakic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alcon Laboratories, Inc.

Sources (1)

  • FDA UDI ab0b0f3a-c111-429f-a2e1-194c1f3e2cc7 35 fields · synced May 31, 2026