Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007190523

FEI Number

3007190523

Entity Name

EVERGREEN ORTHOPEDIC RESEARCH LAB

City/State/Country

Kirkland, WA, US

Establishment Address

Building W, 11317 NE 120th St, Kirkland, WA 98034, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Evergreen Orthopedic Research Lab (Owner Number: 10026600)

Owner / Operator Contact Address

11317 NE 120th St, Building W, Kirkland, WA 98034, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Precision Pin Smooth Pin Precision Stop Pin Fluted Threaded Pin Universal Pin Fluted Pin Straight Hohman Retractor Angled Hohman Retractor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HTW	Bit, Drill	Orthopedic	Class 1	888.4540	2008-08-04
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2008-08-04
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2008-08-04

Official Correspondent

Jeff Stepanian

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Evergreen Orthopedic Research Lab

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

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3011577940	Titan Spine, a Division of Medtronic	Milwaukee, WI, US
2031917	CLASSIC WIRE CUT COMPANY, INC.	Valencia, CA, US
3003431869	HILBRO INTERNATIONAL (PVT) LIMITED	SIALKOT Punjab, PK
3023265483	PHEN'X TECHNOLOGIES	Chassieu Auvergne-Rhone-Alpes, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007190523. Last updated year: 2026. Please use registration number 3007190523 when referencing this establishment in official correspondence.