Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012500984

FEI Number

3012500984

Entity Name

SEGUE XIAMEN MANUFACTURING SERVICES, INC

City/State/Country

Xiamen Fujian, CN

Establishment Address

3/4F #47 2nd South Haijing Rd, Haicang District, Xiamen Fujian 361026, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Segue Xiamen Manufacturing Services, Inc (Owner Number: 10083975)

Owner / Operator Contact Address

3/4F #47 2nd South Haijing Rd, Haicang District, Xiamen, CN-FJ 361026, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Johnson & Johnson

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ORZ	Eyelid Thermal Pulsation System	Ophthalmic	Class 2	886.5200	2022-01-05

Official Correspondent

Joe Yang

US Agent Details

Stephanie Lin Business: Segue Manufacturing Services Email: stephanie.lin@us.lisconn.com Phone: (610) 7398692

Related Public Records

Same Entity

Segue Xiamen Manufacturing Services, Inc

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 3012500984. Last updated year: 2026. Please use registration number 3012500984 when referencing this establishment in official correspondence.