Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012387552

FEI Number

3012387552

Entity Name

JAYWAVE INC.

City/State/Country

Gimpo-si Gyeonggi, KR

Establishment Address

74, Hwanggeum-ro, 109beon-gil, Yangchon-eup, Gimpo-si Gyeonggi 10048, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Jaywave Inc. (Owner Number: 10095622)

Owner / Operator Contact Address

74, Hwanggeum-ro, 109beon-gil, Yangchon-eup, Gimpo-si, KR-41 10048, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DUODERM PATCH DUODERM BANDAGE

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2026-04-03

Official Correspondent

Patty Min

US Agent Details

Joyce Kwon Business: PROVISION CONSULTING GROUP, INC. Email: ask@provisionfda.com Phone: (909) 4933276

Related Public Records

Same Entity

Jaywave Inc.

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 3012387552. Last updated year: 2026. Please use registration number 3012387552 when referencing this establishment in official correspondence.