BLUEOCEAN GLOBAL CORP

FDA Device Registration & Listing · Southold, NY, US · Registration 3028117759

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
3028117759
FEI Number
3028117759
Entity Name
BLUEOCEAN GLOBAL CORP
City/State/Country
Southold, NY, US
Establishment Address
370 Koke Drive, Southold, NY 11971, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
BlueOcean Global Corp (Owner Number: 10088550)
Owner / Operator Contact Address
12550 Biscayne Blvd, Suite 110, Miami, FL 33181, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K253291
PMA Number
N/A

All Registered Proprietary Names

Excelsior System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Orthopedic Class 2 888.3030 2026-01-23

Official Correspondent

Robert Ludecker

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BlueOcean Global Corp
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
K033476 Howmedica Osteonics Corp. MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM 2004-01-20

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3028117759. Last updated year: 2026. Please use registration number 3028117759 when referencing this establishment in official correspondence.
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