Boyd Technologies (Thailand) Co., Ltd.

FDA Device Registration & Listing · Amphur Muang Chonburi Chon Buri, TH · Registration 3014640930

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
3014640930
FEI Number
3014640930
Entity Name
Boyd Technologies (Thailand) Co., Ltd.
City/State/Country
Amphur Muang Chonburi Chon Buri, TH
Establishment Address
700/675, 700/677 Moo 7, Tambol Donhualo, Amphur Muang Chonburi Chon Buri 20000, TH
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Boyd Corporation (Owner Number: 10058271)
Owner / Operator Contact Address
700/675, 700/677 Moo 7, Tambol Donhualo,, Amphur Muang Chonburi, TH-20 20000, TH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Vital Patch

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency Cardiovascular Class 2 870.2910 2022-05-10

Official Correspondent

No official correspondent registered.

US Agent Details

Chris Cook Email: chris.cook@boydcorp.com Phone: (503) 9139641

Related Public Records

Same Entity

Boyd Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3021090069 BOYD CORPORATION Juarez Chihuahua, MX

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K131913 Philips Medizin Systeme Boeblingen GmbH INTELLIVUE CL SPO2 POD AND CL NBP POD, PHILIPS INTELLIVUE PATIENT MONITORS MP5, MP5T, MP5SC 2013-11-26

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014640930. Last updated year: 2026. Please use registration number 3014640930 when referencing this establishment in official correspondence.
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