WEST COAST SURGICAL LLC.

FDA Device Registration & Listing · Half Moon Bay, CA, US · Registration 3005619998

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
3005619998
FEI Number
3005619998
Entity Name
WEST COAST SURGICAL LLC.
City/State/Country
Half Moon Bay, CA, US
Establishment Address
141 California Ave, Suite 101, Half Moon Bay, CA 94019, 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
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

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

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HAO Instrument, Surgical, Non-Powered Neurology Class 1 882.4535 2006-03-01
KTZ Caliper Orthopedic Class 1 888.4150 2006-12-19
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2006-03-01
FWZ Operating Room Accessories Table Tray General, Plastic Surgery Class 1 878.4950 2009-10-21
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 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
3015425095 West Coast Surgical LLC Houston, TX, 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.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005619998. Last updated year: 2026. Please use registration number 3005619998 when referencing this establishment in official correspondence.
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