AVEFLOR

FDA Device Registration & Listing · Kopidlno Jicin, CZ · Registration 3011801804

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
3011801804
FEI Number
3011801804
Entity Name
AVEFLOR
City/State/Country
Kopidlno Jicin, CZ
Establishment Address
Budceves 26, Kopidlno Jicin 507 32, CZ
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Aveflor (Owner Number: 10049570)
Owner / Operator Contact Address
Budceves 26, Kopidlno, CZ-522 507 32, CZ
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

NIX ULTRA 100ML RID SUPER MAX SENSITIVE SKIN SOLUTION RID SUPER MAX ADVANCED SHAMPOO KIT RID SUPER MAX SENSITIVE SKIN KIT RID SUPER MAX ADVANCED SHAMPOO

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LJL Detectors And Removers, Lice, (Including Combs) General Hospital Class 1 880.5960 2020-11-04
PUN Lice Removal Kit Containing A Solution General Hospital Class 1 880.5960 2025-03-25

Official Correspondent

Jan Zubaty

US Agent Details

FDAIMPORTS.COM LLC Email: registration@fdaimports.com Phone: (410) 2202800

Related Public Records

Same Entity

Aveflor
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 3011801804. Last updated year: 2026. Please use registration number 3011801804 when referencing this establishment in official correspondence.
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