Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015425095

FEI Number

3015425095

Entity Name

West Coast Surgical LLC

City/State/Country

Houston, TX, US

Establishment Address

10727 Kinghurst Drive, Houston, TX 77099, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

WEST COAST SURGICAL LLC. (Owner Number: 9083664)

Owner / Operator Contact Address

141 California Ave, Suite 101, Half Moon Bay, CA 94019, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TRAY, SURGICAL, INSTRUMENT Accessory Holding Arm INSTRUMENT, SURGICAL, NON-POWERED ORTHOPEDIC MANUAL SURGICAL INSTRUMENT CALIPERS FOR MEASURING BO

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2006-12-19
FWZ	Operating Room Accessories Table Tray	General, Plastic Surgery	Class 1	878.4950	2009-10-21
HAO	Instrument, Surgical, Non-Powered	Neurology	Class 1	882.4535	2006-03-01
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2006-03-01
KTZ	Caliper	Orthopedic	Class 1	888.4150	2006-12-19

Official Correspondent

Devi Lemerand

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WEST COAST SURGICAL LLC.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3005619998	WEST COAST SURGICAL LLC.	Half Moon Bay, CA, US

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
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

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3012574325	HAKAMA AG	Baettwil Solothurn, CH
3001397320	ROECHLING MEDICAL ROCHESTER L.P.	Rochester, NY, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015425095. Last updated year: 2026. Please use registration number 3015425095 when referencing this establishment in official correspondence.