OCEANTRADE INC

FDA Device Registration & Listing · New York, NY, US · Registration 3023662442

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
3023662442
FEI Number
3023662442
Entity Name
OCEANTRADE INC
City/State/Country
New York, NY, US
Establishment Address
228 Park Ave S Pmb 78258, New York, NY 10003, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
OCEANTRADE INC (Owner Number: 10093918)
Owner / Operator Contact Address
228 PARK AVE S #78258, New York, NY 10003, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Silicone Adult Products Medical crutches

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDA Elastomer, Silicone, For Scar Management General, Plastic Surgery Class 1 878.4025 2025-08-05
IPR Crutch Physical Medicine Class 1 890.3150 2025-08-05

Official Correspondent

Bill Zhang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

OCEANTRADE INC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023662442. Last updated year: 2026. Please use registration number 3023662442 when referencing this establishment in official correspondence.
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