Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014611360

FEI Number

3014611360

Entity Name

VITRO S.A.

City/State/Country

Sevilla, ES

Establishment Address

C/ Luis Fuentes Bejarano, 60 - Edif. Nudo Norte (Local 3), Sevilla 41020, ES

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Vitro S.A. (Owner Number: 10090960)

Owner / Operator Contact Address

C/ Luis Fuentes Bejarano, 60 - Edif. Nudo Norte (Local 3), Sevilla, ES-SE 41020, ES

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VitroStainer_42 NeoPath Pro Vitro TBS Tween 20 Buffer 10X NeoPath Pro Vitro

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KPA	Slide Stainer, Automated	Pathology	Class 1	864.3800	2024-06-07
JCC	Ph Buffer	Pathology	Class 1	864.4010	2024-11-07

Official Correspondent

Alberto Roncero Franco

US Agent Details

Gina Redden Business: Coda Corp USA Email: GGuidoredden@CodaCorpUSA.com Phone: (716) 5502579

Related Public Records

Same Entity

Vitro S.A.

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 3014611360. Last updated year: 2026. Please use registration number 3014611360 when referencing this establishment in official correspondence.