Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016677053

FEI Number

3016677053

Entity Name

MEDI-TATE

City/State/Country

Hadera Northern, IL

Establishment Address

17 Hauman Street, Hadera Northern 3850169, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Medi-Tate (Owner Number: 10063028)

Owner / Operator Contact Address

17 Hauman Street, Hadera, IL-Z 3850169, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K210138

PMA Number

N/A

All Registered Proprietary Names

iTind iTind iTind Removal Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QKA	Temporarily-Placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia	Gastroenterology, Urology	Class 2	876.5510	2020-03-15
QKA	Temporarily-Placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia	Gastroenterology, Urology	Class 2	876.5510	2021-10-13

Official Correspondent

Ilia Bing

US Agent Details

Elaine Whitmore Business: Scivance Consulting Email: Ejwhitmore@Verizon.Net Phone: (941) 5242546

Related Public Records

Same Entity

Medi-Tate

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 3016677053. Last updated year: 2026. Please use registration number 3016677053 when referencing this establishment in official correspondence.