YOORIM CORP.

FDA Device Registration & Listing · EUMSEONG-GUN Chungbuk, KR · Registration 3003781172

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
3003781172
FEI Number
3003781172
Entity Name
YOORIM CORP.
City/State/Country
EUMSEONG-GUN Chungbuk, KR
Establishment Address
No. 828-10 YANGDUCK-RI, SAMSEONG-MYEON, EUMSEONG-GUN Chungbuk 369-832, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
YOORIM CORP (Owner Number: 9050486)
Owner / Operator Contact Address
828-10 YANGDEOK-RI, SAMSEONG-MYEON,, EUMSEONG-GUN, KR-43 369-832, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

GR Splint SEVEN SPLINT GR Splint Plus GR CAST SEVEN CAST

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2013-09-15
ITG Bandage, Cast Physical Medicine Class 1 890.3025 2004-04-19

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

YOORIM CORP
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3023346034 COMEBETTER (GUANGZHOU) TECHNOLOGY CO., LTD Guangzhou Guangdong, CN
3029961128 GERO3D LTD Tel Aviv-Yafo Central, IL
3043047582 OY PRIMO FINLAND AB Vaasa Pohjanmaa, FI
3018759542 DIMENSION ORTHO Inc. Philadelphia, PA, US
3009605026 JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD. Yancheng Jiangsu, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003781172. Last updated year: 2026. Please use registration number 3003781172 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.