DRYLOCK TECHNOLOGIES LTD

FDA Device Registration & Listing · Eau Claire, WI, US · Registration 3013479058

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
3013479058
FEI Number
3013479058
Entity Name
DRYLOCK TECHNOLOGIES LTD
City/State/Country
Eau Claire, WI, US
Establishment Address
3921 N Hastings Way, Eau Claire, WI 54703, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Drylock Technologies Ltd (Owner Number: 10053727)
Owner / Operator Contact Address
3921 North Hastings Way, Eau Claire, WI 54703, US
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
KME Bedding, Disposable, Medical General Hospital Class 1 880.6060 2017-01-05
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2017-01-05

Official Correspondent

Robert Todahl

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Drylock Technologies Ltd
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 3013479058. Last updated year: 2026. Please use registration number 3013479058 when referencing this establishment in official correspondence.
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