Clareon PanOptix Pro PXYWT5.155

GUDID 00380658437459

CLAREON PANOPTIX PRO TORIC

Alcon Laboratories, Inc.

Posterior-chamber intraocular lens, pseudophakic

• Primary Device ID: 00380658437459
• NIH Device Record Key: 164bccdc-3e56-49df-bdd3-a120e4ec2224
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Clareon PanOptix Pro
• Version Model Number: PXYWT5
• Catalog Number: PXYWT5.155
• Company DUNS: 008018525
• Company Name: Alcon Laboratories, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

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• Device Size Text, specify: 0
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• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00380658437459 [Primary]

FDA Product Code

• MFK: Lens, Multifocal Intraocular

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-03-28
• Device Publish Date: 2025-03-20

On-Brand Devices [Clareon PanOptix Pro]

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• 00380658411008: CLAREON PANOPTIX PRO
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• 00380658436674: CLAREON PANOPTIX PRO TORIC
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• 00380658436575: CLAREON PANOPTIX PRO TORIC
• 00380658436568: CLAREON PANOPTIX PRO TORIC
• 00380658436551: CLAREON PANOPTIX PRO TORIC
• 00380658436544: CLAREON PANOPTIX PRO TORIC
• 00380658436537: CLAREON PANOPTIX PRO TORIC