RAINDROP NEAR VISION INLAY 610-0001 RD1-1

MAUDE Adverse Event Report

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 2018-01-04 for RAINDROP NEAR VISION INLAY 610-0001 RD1-1 manufactured by Revision Optics.

Event Text Entries

[96384178] The inlay remains implanted in the patient's eye and is 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. Glare is listed in the device labeling as a known potential risk. Complaint reference number: (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[96384179] The patient underwent implantation of the raindrop corneal inlay in the left eye on (b)(6) 2016. Postoperatively, the patient reports experiencing significant glare. The patient is also being treated with topical steroids for corneal haze. Additional information has been requested.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005956347-2018-00006
MDR Report Key7164713
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2018-01-04
Date of Report2017-01-04
Date of Event2017-12-05
Date Mfgr Received2017-12-05
Device Manufacturer Date2016-08-22
Date Added to Maude2018-01-04
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. PUSHPITA SINGH
Manufacturer Street25651 ATLANTIC OCEAN DR., STE. A1
Manufacturer CityLAKE FOREST CA 926308835
Manufacturer CountryUS
Manufacturer Postal926308835
Manufacturer Phone9497072740
Manufacturer G1REVISION OPTICS
Manufacturer Street25651 ATLANTIC OCEAN DR., STE. A1
Manufacturer CityLAKE FOREST CA 926308835
Manufacturer CountryUS
Manufacturer Postal Code926308835
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRAINDROP NEAR VISION INLAY
Generic NameCORNEAL INLAY
Product CodeLQE
Date Received2018-01-04
Model Number610-0001
Catalog NumberRD1-1
Lot Number002984
Device Expiration Date2019-08-22
OperatorPHYSICIAN
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerREVISION OPTICS
Manufacturer Address25651 ATLANTIC OCEAN DR., STE. A1 LAKE FOREST CA 926308835 US 926308835


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-01-04

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