Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021218757

FEI Number

3021218757

Entity Name

IDMED CORP.

City/State/Country

San Antonio, TX, US

Establishment Address

401 E Sonterra boulevard, Ste 375, San Antonio, TX 78258, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

IDMED corp. (Owner Number: 10083794)

Owner / Operator Contact Address

401 E Sonterra Boulevard, Ste 375, San Antonio, TX 78258, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NeuroLight ToFscan NeuroLight

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KOI	Stimulator, Nerve, Peripheral, Electric	Anesthesiology	Class 2	868.2775	2021-12-22
HLG	Pupillometer, Ac-Powered	Ophthalmic	Class 1	886.1700	2021-12-22

Official Correspondent

REMI POURCHIER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

IDMED corp.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021218757. Last updated year: 2026. Please use registration number 3021218757 when referencing this establishment in official correspondence.