Primary Device ID | 90818806020527 |
NIH Device Record Key | af55d0a6-24fe-489c-9351-591fa60610ac |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Post Op Spectacle Readers, Lightweight, +2.5 |
Version Model Number | 62025-002 |
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 |
00818806020852 - Light Adjustable Lens (LAL) | 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, 3.0 Diopter |
00818806020869 - Light Adjustable Lens (LAL) | 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, 2.0 Diopter |
00818806020951 - Light Adjustable Lens (LAL) | 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, 1.0 Diopter |
00818806021484 - Light Adjustable Lens (LAL) | 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, 0.0 Diopter |
00818806021736 - Light Adjustable Lens (LAL) | 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, -1.0 Diopter |
00818806021743 - Light Adjustable Lens (LAL) | 2024-12-12 LAL+, Light Adjustable Lens, Sterile, Packaged, -2.0 Diopter |
00818806021019 - RxSight Insertion Device | 2024-11-20 RxSight Insertion Device (Single-Use) |
00818806021378 - Light Adjustable Lens (LAL) | 2023-05-09 LAL+, Light Adjustable Lens, Sterile, Packaged, 4.0 Diopter |