Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3034431159

FEI Number

3034431159

Entity Name

Plexus (Thailand) Co., Ltd.

City/State/Country

Amphur Bang Pakong Chachoengsao, TH

Establishment Address

No. 8/8 Moo 5, Tambol Tha Sa An,, Amphur Bang Pakong Chachoengsao 24130, TH

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

PLEXUS CORP. (Owner Number: 3019588)

Owner / Operator Contact Address

ONE PLEXUS WAY, --, Neenah, WI 54956, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Geri Incubator Geri Incubator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQG	Accessory, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6120	2025-03-09
MTX	Microscope And Microscope Accessories, Reproduction, Assisted	Obstetrics/Gynecology	Class 1	884.6190	2025-03-09
MQG	Accessory, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6120	2025-03-09
MQK	Labware, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6160	2025-03-09

Official Correspondent

No official correspondent registered.

US Agent Details

Scott Theune Business: PLEXUS CORP. Email: scott.theune@plexus.com Phone: (920) 7513571

Related Public Records

Same Entity

PLEXUS CORP.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3011606051	PLEXUS SERVICES RO SRL	Oradea Bihor, RO
3008754394	Plexus Corp. (UK) Limited	Kelso Scottish Borders, The, GB
3006063136	Plexus (Xiamen) Co. Ltd.,	Xiamen, Fujian, CN
2183715	PLEXUS CORP.	Neenah, WI, US
3011120183	Plexus Electronica S. de R.L. de C.V..	Zapopan Jalisco, MX

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0029-2020	CooperSurgical, Inc.	2	Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Frequency Identification (RFID) to detect and monitor all activity in the IVF laboratory. The system helps mitigate the risk of human error every time samples are moved from one dish or tube to another, and safeguards every step of the IVF cycle. While the heated plates comprise a heated composite surface with window for a light source. The heated plates comprise a heated composite surface with window for a light source and either sit on top of existing bench-tops or can be integrated to be flush fitted within workstations. Intended use: Provide a favorable temperature environment for the embryo during the IVF procedure.

Similar Registrations

Registration Number	Establishment Name	Location
3012853704	GENEA BIOMEDX Pty Ltd.	Sydney New South Wales, AU
9680654	WILLIAM A. COOK AUSTRALIA PTY, LTD.	EIGHT MILE PLAINS Queensland, AU
3009747883	Esco Medical Technologies, UAB	Ramuciai Kauno Apskritis, LT
1216677	COOPERSURGICAL, INC.	Trumbull, CT, US
3005580113	COOK MEDICAL LLC	Bloomington, IN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3034431159. Last updated year: 2026. Please use registration number 3034431159 when referencing this establishment in official correspondence.