Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016490370

FEI Number

3016490370

Entity Name

LUCID DIAGNOSTICS, INC.

City/State/Country

Foxborough, MA, US

Establishment Address

200 Foxborough Boulevard, Suite 300, Foxborough, MA 02035, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Lucid Diagnostics, Inc. (Owner Number: 10062329)

Owner / Operator Contact Address

200 Foxborough Boulevard, Suite 300, Foxborough, MA 02035, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K230339

PMA Number

N/A

All Registered Proprietary Names

EsoCheck

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EOX	Esophagoscope (Flexible Or Rigid)	Ear, Nose, Throat	Class 2	874.4710	2023-04-04

Official Correspondent

Matthieu Ennis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lucid Diagnostics, Inc.

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 3016490370. Last updated year: 2026. Please use registration number 3016490370 when referencing this establishment in official correspondence.