F & A FOUNDATION

FDA Device Registration & Listing · Tulsa, OK, US · Registration 3014527966

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014527966
FEI Number
3014527966
Entity Name
F & A FOUNDATION
City/State/Country
Tulsa, OK, US
Establishment Address
6303 E 102nd Street, Tulsa, OK 74137, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
F & A Foundation (dba Reign Medical) (Owner Number: 10057487)
Owner / Operator Contact Address
6303 E 102nd Street, Tulsa, OK 74137, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

CLENCH COMPRESSION STAPLE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JDR Staple, Fixation, Bone Orthopedic Class 2 888.3030 2018-04-13

Official Correspondent

Devin Crawford

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

F & A Foundation (dba Reign Medical)
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
K153770 In2bones Sas OS2(R)-VP Varisation Staple 2016-03-21

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2023 Synthes (USA) Products LLC 2
Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014527966. Last updated year: 2026. Please use registration number 3014527966 when referencing this establishment in official correspondence.
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