Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006973663

FEI Number

3006973663

Entity Name

SCHOTT Technologies Mexico, S.A. de C.V.

City/State/Country

Amatlan de los Reyes Veracruz, MX

Establishment Address

Carretera Mexico-Veracruz Km349 S/N Interior 2 A, Venta Parada, Amatlan de los Reyes Veracruz 94946, MX

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SCHOTT Technologies Mexico, S.A. de C.V. (Owner Number: 10025146)

Owner / Operator Contact Address

Carretera Mexico-Veracruz Km 349 S/N Interior 2 A, Venta Parada, Amatlan de los Reyes, MX-VER 94946, MX

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Stryker Item 0233050400 Stryker Item 0233050490 Stryker Item 0233050300 001388LX9 Surgical Cable 0029009 Surgical Cable Stryker Item 0233035100 Stryker Item 0233035190

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OWN	Confocal Optical Imaging	Gastroenterology, Urology	Class 2	876.1500	2021-05-28
FST	Light, Surgical, Fiberoptic	General, Plastic Surgery	Class 2	878.4580	2017-08-29
FCW	Light Source, Fiberoptic, Routine	Gastroenterology, Urology	Class 2	876.1500	2021-05-26

Official Correspondent

Joshua Beu

US Agent Details

Joshua Beu Business: SCHOTT North America Inc, - Lighting and Imaging Email: joshua.beu@us.schott.com Phone: (508) 9097409

Related Public Records

Same Entity

SCHOTT Technologies Mexico, S.A. de C.V.

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
K260108	Stryker Endoscopy	L12 LED Light Source with AIM	2026-02-12
K191144	Mauna Kea Technologies	Cellvizio 100 Series System with Confocal Miniprobes	2020-01-24
K243591	Optosurgical, LLC	OPTOVISION Endoscopic Light Source Unit	2025-02-19
K901491	Cuda Products Co.	CUDA SURGICAL LIGHT	1990-06-18

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3015612252	INTUITIVE SURGICAL, INC.	Santa Clara, CA, US
3014342096	KARL STORZ SE & CO KG	TUTTLINGEN Baden-Wurttemberg, DE
8010047	OLYMPUS MEDICAL SYSTEMS CORP.	HACHIOJI-SHI Tokyo, JP

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006973663. Last updated year: 2026. Please use registration number 3006973663 when referencing this establishment in official correspondence.