Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013912820

FEI Number

3013912820

Entity Name

FOUNDATION FUSION SOLUTIONS, LLC

City/State/Country

Tulsa, OK, US

Establishment Address

11916 S Oxford Ave, SUITE 206, Tulsa, OK 74137, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Foundation Fusion Solutions, LLC (Owner Number: 10058181)

Owner / Operator Contact Address

11916 S OXFORD AVE, SUITE 206, Tulsa, OK 74137, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CornerLoc TransLoc 3D CornerLoc CornerLoc CornerLoc

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HXB	Probe	Orthopedic	Class 1	888.4540	2018-07-23
OUR	Sacroiliac Joint Fixation	Orthopedic	Class 2	888.3040	2022-09-28
FZX	Guide, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2018-07-23
HTW	Bit, Drill	Orthopedic	Class 1	888.4540	2018-07-23
HWB	Extractor	Orthopedic	Class 1	888.4540	2018-07-23

Official Correspondent

Robert Compton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Foundation Fusion Solutions, LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K213667	SI-BONE, Inc.	iFuse-TORQ® Implant System	2022-06-10

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013912820. Last updated year: 2026. Please use registration number 3013912820 when referencing this establishment in official correspondence.