Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007832484

FEI Number

3007832484

Entity Name

JWP MANUFACTURING

City/State/Country

Santa Clara, CA, US

Establishment Address

3500 Del La Cruz, Santa Clara, CA 95054, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

JWP Manufacturing (Owner Number: 10083322)

Owner / Operator Contact Address

3500 De La Cruz Blvd., 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

AUTOMATED REPROCESSING CONNECTOR SET, 8MM ENDOSCOPE, IS4000

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OUG	Medical Device Data System	General Hospital	Class 1	880.6310	2025-02-07

Official Correspondent

Scott Harney

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JWP Manufacturing

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007832484. Last updated year: 2026. Please use registration number 3007832484 when referencing this establishment in official correspondence.