Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007842980

FEI Number

3007842980

Entity Name

Tortle Products, LLC

City/State/Country

Littleton, CO, US

Establishment Address

9907 Monte Vista Ave, Littleton, CO 80125, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Tortle Product LLC (Owner Number: 10029942)

Owner / Operator Contact Address

9907 Monte Vista Ave, Littleton, CO 80125, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K082367

PMA Number

N/A

All Registered Proprietary Names

Transportle Tortle Products LLC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IKY	Mattress, Flotation Therapy, Non-Powered	General Hospital	Class 1	880.5150	2026-02-05
FRP	Holder, Infant Position	General Hospital	Class 1	880.5680	2009-07-19

Official Correspondent

Jane Scott

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tortle Product LLC

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 3007842980. Last updated year: 2026. Please use registration number 3007842980 when referencing this establishment in official correspondence.