Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042639641

FEI Number

3042639641

Entity Name

SPLINTBOX

City/State/Country

Frontenac, MO, US

Establishment Address

3 Clayton Ter, Frontenac, MO 63131, US

Establishment Type(s)

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

Owner / Operator

SplintBox (Owner Number: 10094826)

Owner / Operator Contact Address

7750 Maryland Ave, PO Box 11353, Clayton, MO 63105, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SplintBox VSS SplintBox LLS SplintBox GSS SplintBox STS SplintBox SLS SplintBox PSS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ITG	Bandage, Cast	Physical Medicine	Class 1	890.3025	2025-12-26

Official Correspondent

Alex Poague

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SplintBox

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 3042639641. Last updated year: 2026. Please use registration number 3042639641 when referencing this establishment in official correspondence.