SURFACIDE, LLC.

FDA Device Registration & Listing · Waukesha, WI, US · Registration 3013869012

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
3013869012
FEI Number
3013869012
Entity Name
SURFACIDE, LLC.
City/State/Country
Waukesha, WI, US
Establishment Address
N16w23390 Stone Ridge Dr Ste G, Waukesha, WI 53188, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Surfacide, LLC. (Owner Number: 10095730)
Owner / Operator Contact Address
N16W23390 Stone Ridge Dr Suite G, Waukesha, WI 53188, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K242604
PMA Number
N/A

All Registered Proprietary Names

Helios+ UV-C System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QXJ Whole Room Microbial Reduction Device General Hospital Class 2 880.6510 2026-04-20

Official Correspondent

Gunner Lyslo

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Surfacide, LLC.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013869012. Last updated year: 2026. Please use registration number 3013869012 when referencing this establishment in official correspondence.
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