Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015745793

FEI Number

3015745793

Entity Name

DRYLOCK TECHNOLOGIES S.R.L.

City/State/Country

Buccinasco Milano, IT

Establishment Address

Via delle Azalee 13, Buccinasco Milano 20090, IT

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Foreign Private Label Distributor,Manufacture Medical Device

Owner / Operator

Drylock Technologies S.r.l. (Owner Number: 10061000)

Owner / Operator Contact Address

Via delle Azalee 13, Buccinasco, IT-MI 20090, IT

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2019-08-01
NRC	Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile	Obstetrics/Gynecology	Class 1	884.5425	2021-12-02

Official Correspondent

Chiara Fazio

US Agent Details

Robert Todahl Business: Quality Manager Email: robert.todahl@drylocktechnologies.com Phone: (715) 2801725

Related Public Records

Same Entity

Drylock Technologies S.r.l.

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 3015745793. Last updated year: 2026. Please use registration number 3015745793 when referencing this establishment in official correspondence.