RxSight Contact Lens

GUDID 00818806021774

RxSight Contact Lens

RXSIGHT, INC.

Vitrectomy contact lens, reusable

• Primary Device ID: 00818806021774
• NIH Device Record Key: 5d95aa1b-66dc-45ec-b15d-0f0b12feecd8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RxSight Contact Lens
• Version Model Number: 62020-002
• Company DUNS: 052054413
• Company Name: RXSIGHT, 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: 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	00818806021774 [Primary]

FDA Product Code

• HJK: Lens, Contact, Polymethylmethacrylate, Diagnostic

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: 2025-09-15
• Device Publish Date: 2025-09-05

On-Brand Devices [RxSight Contact Lens]

• 00818806020531: RxSight Contact Lens
• 00818806021774: RxSight Contact Lens