Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014650073

FEI Number

3014650073

Entity Name

Silq Technologies Corporation

City/State/Country

Sunny Isles Beach, FL, US

Establishment Address

323 Sunny Isles Blvd., 7th Floor, Sunny Isles Beach, FL 33160, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Silq Technologies Corporation (Owner Number: 10077941)

Owner / Operator Contact Address

323 Sunny Isles Blvd., 7th Floor, Sunny Isles Beach, FL 33160, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K192034

PMA Number

N/A

All Registered Proprietary Names

2-Way 100% Silicone, 18Fr X 10ml, ClearTract SPT Catheter 2-Way 100% Silicone, 14Fr X 10ml, ClearTract SPT Catheter 2-Way 100% Silicone, 16Fr X 5ml, ClearTract SPT Catheter 2-Way 100% Silicone, 16Fr X 10ml, ClearTract SPT Catheter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EZL	Catheter, Retention Type, Balloon	Gastroenterology, Urology	Class 2	876.5130	2020-10-12

Official Correspondent

D. Verne Sharma

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Silq Technologies Corporation

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
K233013	Silq Technologies Corporation	2-Way 100% Silicone Cleartract Catheter	2024-01-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014650073. Last updated year: 2026. Please use registration number 3014650073 when referencing this establishment in official correspondence.