Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022764278

FEI Number

3022764278

Entity Name

EndoTheia, Inc.

City/State/Country

Nashville, TN, US

Establishment Address

201 25th Ave South, Nashville, TN 37203, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

EndoTheia, Inc. (Owner Number: 10093173)

Owner / Operator Contact Address

201 25th Ave South, Nashville, TN 37203, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

FlexStone Basket

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FFL	Dislodger, Stone, Basket, Ureteral, Metal	Gastroenterology, Urology	Class 2	876.4680	2025-04-10

Official Correspondent

Christopher Schlichter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EndoTheia, 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 3022764278. Last updated year: 2026. Please use registration number 3022764278 when referencing this establishment in official correspondence.