Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010849408

FEI Number

3010849408

Entity Name

CELESTICA

City/State/Country

Valencia, ES

Establishment Address

Carretera Valencia-Ademuz km 17,6, 46185 La Pobla de Vallbona, Valencia 46185, ES

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Celestica (Owner Number: 10057437)

Owner / Operator Contact Address

Carretera Valencia-Ademuz km 17,6, 46185 La Pobla de Vallbona, Valencia, ES-V 46185, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Bodyport Cardiac Scale Aveir Patient Transmitter Model LSRM01 Sterilizable Cord for Electric Power Supply

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DSB	Plethysmograph, Impedance	Cardiovascular	Class 2	870.2770	2023-03-28
PNJ	Leadless Pacemaker	Cardiovascular	Class 3	870.3610	2025-01-08
HQF	Laser, Ophthalmic	Ophthalmic	Class 2	886.4390	2025-05-13
HAB	Saw, Powered, And Accessories	General, Plastic Surgery	Class 1	878.4820	2025-02-13

Official Correspondent

Gonzalo Encinas

US Agent Details

Payal Copling Email: payal.copling@celestica.com Phone: (469) 3953251

Related Public Records

Same Entity

Celestica

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K834060	F. & F. Koenigkramer	RELIANCE OPHTHALMIC SLIT LAMP R-083	1984-02-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0753-2025	Abbott Medical	3	The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming system which operates using the Merlin PCS Model 3330 software and is designed to interrogate, program, display data from, and test Abbott Medical implantable devices and leads.
Z-1557-2025	Abbott Medical	3	Aveir DR Leadless Pacemaker (LP) Ventricular Device REF LSP202V UDI-DI code: 05415067040725 REF LSP112V UDI-DI code: 05415067034472 The Aveir leadless pacemaker system supports the implantation and use of an Aveir Leadless Pacemaker (LP) within the targeted chamber(s) of the heart for monitoring a patient s heart rate and providing rate responsive bradycardia pacing therapy to regulate heart rate.
Z-1695-2024	Abbott Medical	3	Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO

Similar Registrations

Registration Number	Establishment Name	Location
2025475	VALHALLA SCIENTIFIC, INC.	Poway, CA, US
3004987887	USCOM LIMITED	SYDNEY New South Wales, AU
3009156722	SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.	Shenzhen Guangdong, CN
3004782476	Impedimed Limited	Lindfield New South Wales, AU
3007305624	GUANGDONG BIOLIGHT MEDITECH CO., LTD	Zhuhai Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010849408. Last updated year: 2026. Please use registration number 3010849408 when referencing this establishment in official correspondence.