510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K253704Substantially Equivalent

iPredict-DR

iHealthscreen, Inc., Richmond Hill NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K253704 is the FDA 510(k) clearance record for iPredict-DR, a class II device, cleared for iHealthscreen, Inc. on under FDA product code PIB (Diabetic Retinopathy Detection Device). FDA's definition for product code PIB reads: "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". FDA records list one 510(k) clearance for iHealthscreen, Inc. As of , FDA records show no recalls naming K253704.

Clearance record

Decision date
Received
(220 days to decision)
Product code
PIB Diabetic Retinopathy Detection Device
Regulation
21 CFR 886.1100
Device class
Class II
Review panel
Ophthalmic
Applicant
iHealthscreen, Inc. 132-02 89th Ave., Suite 214, Richmond Hill NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code PIB

Trailing 12 months
1 clearance under product code PIB in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code PIB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260