Post Op Spectacle Readers, Lightweight, +1.50

GUDID 90818806020510

Post Op Spectacle Readers, Lightweight, +1.50

RXSIGHT, INC.

Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted spectacle lens, non-prescription Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens

• Primary Device ID: 90818806020510
• NIH Device Record Key: 8bd41fff-d822-4929-90ab-bb8133e89e0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Post Op Spectacle Readers, Lightweight, +1.50
• Version Model Number: 62025-001
• Company DUNS: 052054413
• Company Name: RXSIGHT, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	90818806020510 [Primary]

FDA Product Code

• HQY: Sunglasses (Non-Prescription Including Photosensitive)

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-08
• Device Publish Date: 2020-09-30

Devices Manufactured by RXSIGHT, INC.

• 00818806021378 - Light Adjustable Lens (LAL): 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 4.0 Diopter
• 00818806021385 - Light Adjustable Lens (LAL): 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 5.0 Diopter
• 00818806021392 - Light Adjustable Lens (LAL): 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 6.0 Diopter
• 00818806021408 - Light Adjustable Lens (LAL): 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 7.0 Diopter
• 00818806021415 - Light Adjustable Lens (LAL): 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 8.0 Diopter
• 00818806021422 - Light Adjustable Lens (LAL): 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 9.0 Diopter
• 00818806021439 - Light Adjustable Lens (LAL): 2023-05-09 LAL, Sterile, Packaged, 5.0 Diopter
• 00818806021446 - Light Adjustable Lens (LAL): 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 11.0 Diopter