ENDEAVOR ORTHOPAEDICS. LLC

FDA Device Registration & Listing · Tulsa, OK, US · Registration 3021349259

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
3021349259
FEI Number
3021349259
Entity Name
ENDEAVOR ORTHOPAEDICS. LLC
City/State/Country
Tulsa, OK, US
Establishment Address
8516 E 101st St, Suite A, Endeavor Office, Tulsa, OK 74133, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Endeavor Orthopaedics. LLC (Owner Number: 10083956)
Owner / Operator Contact Address
11601 S. Richmond Ave, Tulsa, OK 74137, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K203408
PMA Number
N/A

All Registered Proprietary Names

Summit Patella Plating System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HRS Plate, Fixation, Bone Orthopedic Class 2 888.3030 2022-01-04
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2022-01-04

Official Correspondent

Dana Funk

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Endeavor Orthopaedics. 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
K042598 Zimmer, Inc. PERIARTICULAR LOCKING PLATES AND SCREWS, 2357 AND 2359 SERIES 2004-10-29
K190842 Jiangsu Trauhui Medical Instrument Co., Ltd. Comus Locking Plate systems 2020-02-03
K130510 Arthrex, Inc. ARTHREX COMPRESSION PLATES 2013-09-25
K202803 Newclip Technics Activmotion S DTO 2021-12-16
K072322 Smith & Nephew, Inc. ULTRA FAST-FIX AND ULTRA FAST-FIX AB MENISCAL REPAIR SYSTEMS 2007-09-18

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0034-2022 Flower Orthopedics Corporation 2
Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021349259. Last updated year: 2026. Please use registration number 3021349259 when referencing this establishment in official correspondence.
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