SEACOMP DISPLAYS

FDA Device Registration & Listing · Tijuana Baja California, MX · Registration 3033509895

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
3033509895
FEI Number
3033509895
Entity Name
SEACOMP DISPLAYS
City/State/Country
Tijuana Baja California, MX
Establishment Address
Andador Vecinal 15801, Fraccionamiento el Rosario, Tijuana Baja California 22675, MX
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Seacomp Displays (Owner Number: 10091907)
Owner / Operator Contact Address
Andador Vecinal 15801, Fraccionamiento el Rosario, Tijuana, MX-BCN 22675, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ActivForce 2 PIvot Breath Sensor UrinDx REMI Remote EEG Monitoring System Activforce 2

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QNO Neuromuscular Tongue Muscle Stimulator For The Reduction Of Snoring And Obstructive Sleep Apnea Dental Class 2 872.5575 2025-11-28
HRW Dynamometer, Nonpowered Orthopedic Class 1 888.1250 2024-11-14
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase Anesthesiology Class 2 868.1430 2024-12-13
KQO Automated Urinalysis System Clinical Chemistry Class 1 862.2900 2026-03-04
OMC Reduced- Montage Standard Electroencephalograph Neurology Class 2 882.1400 2025-03-06
GXY Electrode, Cutaneous Neurology Class 2 882.1320 2025-03-06
KQX Goniometer, Ac-Powered Orthopedic Class 1 888.1500 2025-12-04

Official Correspondent

Ramiro Ornelas Chan

US Agent Details

Erik Sierks Business: Seacomp Email: erik.sierks@seacomp.com Phone: (224) 7158811

Related Public Records

Same Entity

Seacomp Displays
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
K101852 Iris International Inc., A Division of Iris Iris I CHEM VELOCITY AUTOMATED URINE CHEMISTRY SYSTEM, STRIPS AND CALCHEK KIT 2011-03-23
K070612 Top-Rank Health Care Equipment Co., Ltd. TOP-RANK ADHESIVE ELECTRODE 2007-05-07
K123915 Grass Technologies, an Astro-Med, Inc. Product Gro DE48-PLUS 2013-04-24
K073532 Technomed Europe DISPOSABLE ADHESIVE SURFACE ELECTRODES, DISC ELECTRODES 2008-05-01
K260363 Ceribell, Inc. Ceribell Brain Monitor Headband 2026-04-03

Similar Registrations

Registration Number Establishment Name Location
3017737771 SIGNIFIER MEDICAL TECHNOLOGIES LLC Wake Forest, NC, US
3013445086 FREUDENBERG MEDICAL EUROPE GMBH Kaiserslautern Rhineland-Palatinate, DE
3018192374 SIGNIFIER MEDICAL TECHNOLOGIES LIMITED London London, City of, GB
3017430550 MILLI-HENRY ELECTRONICS CO., LTD. Dongguan Guangdong, CN
3030154802 HANDEXER LLC South El Monte, CA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033509895. Last updated year: 2026. Please use registration number 3033509895 when referencing this establishment in official correspondence.
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