BILKIM LTD CO.

FDA Device Registration & Listing · IZMIR, TR · Registration 3005391797

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
3005391797
FEI Number
3005391797
Entity Name
BILKIM LTD CO.
City/State/Country
IZMIR, TR
Establishment Address
Kazim Pasa Mahallesi, 1212/1 Sokak, No:1- 1/1, 35660 Menemen, IZMIR 35660, TR
Establishment Type(s)
Foreign Private Label Distributor,Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
BILKIM LTD CO. (Owner Number: 10040579)
Owner / Operator Contact Address
Kazim Pasa Mahallesi, 1212/1 Sokak, No:1- 1/1, 35660 Menemen, IZMIR, TR-35 35660, TR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

WAX, DENTAL, INTRAORAL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EGD Wax, Dental, Intraoral Dental Class 1 872.6890 2012-04-26

Official Correspondent

Jenny Sohn

US Agent Details

Jenny Sohn Email: jsohn727@gmail.com Phone: (646) 2637753

Related Public Records

Same Entity

BILKIM LTD CO.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3001122163 KENT MANUFACTURING COMPANY Grand Rapids, MI, US
3009426332 GARRECO, LLC Heber Springs, AR, US
1821514 KULZER, LLC SOUTH BEND, IN, US
3004623350 ASHTEL STUDIOS, INC. Ontario, CA, US
3022519816 SHENZHEN YONGCHANGHE TECHNOLOGY CO., LTD. Shenzhen Guangdong, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005391797. Last updated year: 2026. Please use registration number 3005391797 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.