DRYLOCK TECHNOLOGIES SL.

FDA Device Registration & Listing · Hontoria Segovia, ES · Registration 3016640796

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
3016640796
FEI Number
3016640796
Entity Name
DRYLOCK TECHNOLOGIES SL.
City/State/Country
Hontoria Segovia, ES
Establishment Address
C/ Gremio de los Cordeleros N 1, Hontoria Segovia 40195, ES
Establishment Type(s)
Foreign Private Label Distributor,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Drylock Technologies SL. (Owner Number: 10087117)
Owner / Operator Contact Address
C/ Gremio de los Cordeleros N 1, Hontoria, ES-SG 40195, ES
Initial Importer Flag
N
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 2023-01-13
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2023-06-22
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2023-06-22

Official Correspondent

Marta Arranz

US Agent Details

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

Related Public Records

Same Entity

Drylock Technologies SL.
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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016640796. Last updated year: 2026. Please use registration number 3016640796 when referencing this establishment in official correspondence.
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