Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030444864

FEI Number

3030444864

Entity Name

PLANDOCS INC.

City/State/Country

Seoul, KR

Establishment Address

Baegjegobunlo248, Songpa-gu, Seoul 05584, KR

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Foreign Private Label Distributor

Owner / Operator

Plandocs Inc. (Owner Number: 10092732)

Owner / Operator Contact Address

Baegjegobunlo248, Songpa-gu, Seoul, KR-11 05584, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PD NANO CANNULA

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GEA	Cannula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2025-02-12

Official Correspondent

Myong Su Choe

US Agent Details

Jamie Park Business: Plandocs USA, Inc. Email: jamie@plandocsusa.com Phone: (201) 8151740

Related Public Records

Same Entity

Plandocs Inc.

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
K863293	Lifestream Int'L, Inc.	DISPOSABLE SUCTION CANNULA NO. 902008-000	1986-09-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030444864. Last updated year: 2026. Please use registration number 3030444864 when referencing this establishment in official correspondence.