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Data / Medical devices / Czechia / Drylock Technologies S.R.O.

Drylock Technologies S.R.O.: FDA-registered device maker in Hradek nad Nisou Liberecky Kraj, Czechia, 1 510(k) clearance

Drylock Technologies S.R.O. is registered with the FDA (registration 3012387254) in Hradek nad Nisou Liberecky Kraj, Czechia. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated April 16, 1982. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012387254
Address
Vlamska 801, Hradek nad Nisou Liberecky Kraj, Czechia, 46334
Owner or operator
Drylock Technologies s.r.o. (10076959)
Roles
Contract manufacturer, Manufacturer
First device listed
August 6, 2020
Registered through
2026
Brand names listed
Invizi Guards, Invizi Pads, Invizi Pants, Invizi Slips, LI Nexwear Perf Extra Plus 30, LI Nexwear Prem Extra 30, LI Nexwear Prem Normal 30, Nundies Youth Pants

Devices it lists

DeviceProduct codeClassRoleSource
Garment, Protective, For IncontinenceEYQ1Contract manufacturer, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
April 16, 1982K820961INCONTINENCE PAD OR ADULT DIAPEREYQSubstantially EquivalentDafoe & Dafoe, Inc.accessdata.fda.gov

Compare with other makers

Updated April 16, 1982. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.