Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030686085

FEI Number

3030686085

Entity Name

G-TECH MEDICAL Inc.

City/State/Country

Mountain View, CA, US

Establishment Address

2495 Hospital Dr Ste 300, Mountain View, CA 94040, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

G-Tech Medical (Owner Number: 10090462)

Owner / Operator Contact Address

2495 Hospital Drive, Suite 300, Mountain View, CA 94040, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K212954

PMA Number

N/A

All Registered Proprietary Names

GutTracker

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MYE	System, Electrogastrography (Egg)	Gastroenterology, Urology	Class 2	876.1735	2024-04-01

Official Correspondent

Robert Kirby

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

G-Tech Medical

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 3030686085. Last updated year: 2026. Please use registration number 3030686085 when referencing this establishment in official correspondence.