Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022298582

FEI Number

3022298582

Entity Name

D3D,LLC

City/State/Country

Sioux Falls, SD, US

Establishment Address

3617 N 1st Ave, Sioux Falls, SD 57104, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

D3D,LLC (Owner Number: 10084811)

Owner / Operator Contact Address

3617 N. 1st Ave, Sioux Falls, SD 57104, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sternum Protect Pad Sternum Protect Sternum Protector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMO	Binder, Elastic	General Hospital	Class 1	880.5160	2022-04-03

Official Correspondent

Angel Rollag

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

D3D,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 3022298582. Last updated year: 2026. Please use registration number 3022298582 when referencing this establishment in official correspondence.