Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011459762

FEI Number

3011459762

Entity Name

FABRINET WEST

City/State/Country

Santa Clara, CA, US

Establishment Address

4900 Patrick Henry Drive, Santa Clara, CA 95054, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Fabrinet West (Owner Number: 10060996)

Owner / Operator Contact Address

4900 Patrick Henry Drive, Santa Clara, CA 95054, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Intuitive Surgical, Inc.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAY	System, Surgical, Computer Controlled Instrument	Gastroenterology, Urology	Class 2	876.1500	2019-07-25

Official Correspondent

Prabhjot Paul

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fabrinet West

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3013942591	INTUITIVE SURGICAL, INC.	Sunnyvale, CA, US
3009941480	LISI MEDICAL REmmele	Big Lake, MN, US
3015612252	INTUITIVE SURGICAL, INC.	Santa Clara, CA, US
3013283620	Intuitive Surgical G.K.	Tokyo, JP
3007593944	Asensus Surgical, Inc.	Morrisville, NC, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011459762. Last updated year: 2026. Please use registration number 3011459762 when referencing this establishment in official correspondence.