Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021242837

FEI Number

3021242837

Entity Name

SEEMEDX, INC

City/State/Country

Las Vegas, NV, US

Establishment Address

6280 S Valley View Blvd., Suite 632, Las Vegas, NV 89118, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Seemedx, Inc (Owner Number: 10083858)

Owner / Operator Contact Address

6280 S Valley View Blvd., Suite 632, Las Vegas, NV 89118, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K133301

PMA Number

N/A

All Registered Proprietary Names

ZOE Fluid Status Monitor ZOE Fluid Status Monitor ZOE Fluid Status Monitor ZOE Fluid Status Monitor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DSB	Plethysmograph, Impedance	Cardiovascular	Class 2	870.2770	2021-12-23
DSB	Plethysmograph, Impedance	Cardiovascular	Class 2	870.2770	2021-12-23
DSB	Plethysmograph, Impedance	Cardiovascular	Class 2	870.2770	2021-12-23
DSB	Plethysmograph, Impedance	Cardiovascular	Class 2	870.2770	2021-12-23

Official Correspondent

Philip Hamski

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Seemedx, Inc

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

View Entity Profile →

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3004782476	Impedimed Limited	Lindfield New South Wales, AU
3007305624	GUANGDONG BIOLIGHT MEDITECH CO., LTD	Zhuhai Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021242837. Last updated year: 2026. Please use registration number 3021242837 when referencing this establishment in official correspondence.