RETMAP, INC.

FDA Device Registration & Listing · Chicago, IL, US · Registration 3033274216

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3033274216
FEI Number
3033274216
Entity Name
RETMAP, INC.
City/State/Country
Chicago, IL, US
Establishment Address
832 W Superior St # 202e, Chicago, IL 60642, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
RetMap, Inc. (Owner Number: 10091755)
Owner / Operator Contact Address
832 W Superior St, 202E, Chicago, IL 60642, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K253586
PMA Number
N/A

All Registered Proprietary Names

RM Electrode RM Electrode (Model Number: RMH 25-01)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HLZ Electrode, Corneal Ophthalmic Class 2 886.1220 2024-10-30
HLZ Electrode, Corneal Ophthalmic Class 2 886.1220 2026-06-08

Official Correspondent

Shresta Patangay

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RetMap, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033274216. Last updated year: 2026. Please use registration number 3033274216 when referencing this establishment in official correspondence.
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