MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-01-17 for RAINDROP NEAR VISION INLAY 610-0001 RD1-1 manufactured by Revision Optics.
[97633924]
The explanted corneal inlay was lost during handling and was therefore not available for evaluation. The device history record review of the manufacturing lot for this device was performed and there were no discrepancies or unusual findings related to the reported issue. Inlay shifts in position and decreased vision are listed in the device labeling as known potential risks. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[97633925]
The patient underwent implantation of the raindrop corneal inlay in the right eye on (b)(6) 2017. Postoperatively the inlay decentered 2 mm inferiorly. In addition, the patient's best corrected distance visual acuity (bcdva) decreased from 20/20 (preoperatively) to 20/30 immediately prior to inlay explantation on (b)(6) 2017. According to the surgeon, poor fixation during surgery was a contributing factor. At last examination on (b)(6) 2018, bcdva improved to 20/20 with a bandage contact lens in place and the patient was reported as stable.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3005956347-2018-00013 |
| MDR Report Key | 7202701 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2018-01-17 |
| Date of Report | 2018-01-17 |
| Date of Event | 2017-12-27 |
| Date Mfgr Received | 2017-12-19 |
| Device Manufacturer Date | 2017-05-12 |
| Date Added to Maude | 2018-01-17 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. PUSHPITA SINGH |
| Manufacturer Street | 25651 ATLANTIC OCEAN DR., STE. A1 |
| Manufacturer City | LAKE FOREST CA 926308835 |
| Manufacturer Country | US |
| Manufacturer Postal | 926308835 |
| Manufacturer Phone | 9497072740 |
| Manufacturer G1 | REVISION OPTICS |
| Manufacturer Street | 25651 ATLANTIC OCEAN DR., STE. A1 |
| Manufacturer City | LAKE FOREST CA 926308835 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 926308835 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | RAINDROP NEAR VISION INLAY |
| Generic Name | CORNEAL INLAY |
| Product Code | LQE |
| Date Received | 2018-01-17 |
| Model Number | 610-0001 |
| Catalog Number | RD1-1 |
| Lot Number | 003132 |
| Operator | PHYSICIAN |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | REVISION OPTICS |
| Manufacturer Address | 25651 ATLANTIC OCEAN DR., STE. A1 LAKE FOREST CA 926308835 US 926308835 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2018-01-17 |