Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Product codes
PIB
Product code PIB
Device name
Diabetic Retinopathy Detection Device
Medical specialty
Ophthalmic
Device class
2
Regulation number
886.1100
Review panel
OP
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
N
Summary malfunction reporting
Eligible
Definition
A retinal diagnostic software device is a prescription software device that incorporates an adaptive algorithm to evaluate ophthalmic images for diagnostic screening to identify retinal diseases or conditions.
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K240058
AEYE-DS
Aeye Health, Inc.
2024-04-23
K223357
EyeArt v2.2.0
Eyenuk, Inc.
2023-06-16
K221183
AEYE-DS
Aeye Health, Inc.
2022-11-10
K213037
IDx-DR v2.3
Digital Diagnostics, Inc.
2022-06-17
K203629
IDx-DR
Digital Diagnostics, Inc.
2021-06-10
K200667
EyeArt
Eyenuk, Inc.
2020-08-03
DEN180001
IDx-DR
Idx, LLC
2018-04-11
Related GUDID Devices
#
Primary DI, Brand, Company table
Primary DI
Brand
Company
Published
00850035651032
AEYE Health
Aeye Health, Inc.
2025-02-10
00085003651039
AEYE Health
Aeye Health, Inc.
2024-12-12
00085003651022
AEYE Health
Aeye Health, Inc.
2023-09-28
00850035651001
AEYE Health
Aeye Health, Inc.
2023-07-16
00850035651018
AEYE Health
Aeye Health, Inc.
2023-07-16
00860005195626
IDx-DR
Digital Diagnostics Inc.
2022-06-27
00860005195619
IDx-DR
Digital Diagnostics Inc.
2021-07-09
00860000470001
EyeArt
Eyenuk, Inc.
2020-11-09