Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009662890

FEI Number

3009662890

Entity Name

AMERICAN BENCHMARK MACHINE WORKS

City/State/Country

Olympia, WA, US

Establishment Address

Shop a, 926 79th Ave SE, Olympia, WA 98501, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

American Benchmark Machine Works (Owner Number: 10041048)

Owner / Operator Contact Address

926 Unit A 79th ST SE, Olympia, WA 98501, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Thoracic Pop N' Lock Gearshift Probe Pop N' Lock Thoracic PNL Pop & Lock Lumbar Pop N' Lock PNL Cannulated Probe Lumbar PNL Blue Cozy for Mako Total Knee Bed Arm Clamp Bed Arm Post Airo-Levo Table Adapter Shoulder Positioner Universal Rail Clamp Locking Navigated Stylet & Shunt Passer Navigated Stylet and Shunt Passer Navigated Stylet & Shunt Passer Non-Locking Navigated Stylet and Shunt Passer Non-Locking Navigated Stylet & Shunt Passer Locking Navigated Stylet and Shunt Passer Straight Cutting Awl Trocar Awl Awl Awl Taps Universal Awl Angled Square Awl Angled Awl Beveled Straight Awl Punch Awl Straight Awl

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2015-04-17
JEB	Table, Surgical With Orthopedic Accessories, Manual	General, Plastic Surgery	Class 1	878.4950	2012-06-14
GYK	Instrument, Shunt System Implantation	Neurology	Class 1	882.4545	2017-01-11
HWJ	Awl	Orthopedic	Class 1	888.4540	2012-09-18

Official Correspondent

Steve Jacobson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

American Benchmark Machine Works

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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3027516563	STAR SPORTS MEDICINE CO., LTD.	Beijing, CN
3021574846	3D LOGICS LLC	Hillsboro, OR, US
3030089866	ORTOLOG MEDIKAL SANAYI VE TICARET A.S.	Yenimahalle Ankara, TR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009662890. Last updated year: 2026. Please use registration number 3009662890 when referencing this establishment in official correspondence.