Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3036758824

FEI Number

3036758824

Entity Name

DOIFF CO., LTD.

City/State/Country

Suncheon-si, Jeollanam-do Jeonnam, KR

Establishment Address

82-117, Haeryongsandan 1-ro, Haeryong-myeon, Suncheon-si, Jeollanam-do Jeonnam 58021, KR

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

DOIFF Co., Ltd. (Owner Number: 10092660)

Owner / Operator Contact Address

82-117, Haeryongsandan 1-ro, Haeryong-myeon, Suncheon-si, Jeollanam-do, KR-NOTA 58021, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sinus Simple Kit DSSK01, LCD1525, LCD1828, LCD2228, LCD2535, LCD2838, LCD3238, LCD3545, LCD3848, LCD4248, LCD4555, LCD4858, LCD5258 Aurora / X9, X5, X5 Plus ML100 / ML100A, ML100B

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DZA	Drill, Dental, Intraoral	Dental	Class 1	872.4130	2025-02-04
EAZ	Light, Operating, Dental	Dental	Class 1	872.4630	2025-02-04

Official Correspondent

No official correspondent registered.

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

DOIFF Co., Ltd.

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 3036758824. Last updated year: 2026. Please use registration number 3036758824 when referencing this establishment in official correspondence.