Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043045982

FEI Number

3043045982

Entity Name

BEAUTYXPORT S.R.O.

City/State/Country

Zizkov Praha, Hlavni Mesto, CZ

Establishment Address

Malesicka 2855/2b, Zizkov Praha, Hlavni Mesto 130 00, CZ

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Repack or Relabel Medical Device

Owner / Operator

Beautyxport s.r.o. (Owner Number: 10094944)

Owner / Operator Contact Address

Malesicka 2855/2b, Zizkov, CZ-10 130 00, CZ

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P050047

All Registered Proprietary Names

MONOVISC HYMOVIS JUVEDERM VOLUX with Lidocaine JUVEDERM VOLUMA with Lidocaine JUVEDERM VOLBELLA with Lidocaine SYNVISC ONE RADIESSE 3ml ORTHOVISC RESTYLANE LYFT with Lidocaine RESTYLANE EYELIGHT RADIESSE (+) 1.5ml with Lidocaine RADIESSE 3ml RADIESSE 1.5ml SCULPTRA 2 vials EUFLEXXA DUROLANE RESTYLANE DEFYNE with Lidocaine RESTYLANE KYSSE with Lidocaine RESTYLANE REFYNE with Lidocaine RESTYLANE 1ml with Lidocaine SUPARTZ TEOSYAL RHA2 TEOSYALRHA4 TEOSYAL RHA3 JUVEDERM ULTRA XC JUVEDERM ULTRA PLUS XC

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2026-01-08
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2026-01-08
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-08
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2026-01-09
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-09
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2026-01-08
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-09
PKY	Implant, Dermal, For Aesthetic Use In The Hands	Unknown	Class 3	N/A	2026-01-09
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-08
PKY	Implant, Dermal, For Aesthetic Use In The Hands	Unknown	Class 3	N/A	2026-01-08
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-08
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2026-01-08
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2026-01-08
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-09
MOZ	Acid, Hyaluronic, Intraarticular	Unknown	Class 3	N/A	2026-01-08
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-08
LMH	Implant, Dermal, For Aesthetic Use	Unknown	Class 3	N/A	2026-01-08

Official Correspondent

Ivan Karadhov

US Agent Details

Larry Ordet Business: FDA Solutions Group, LLC Email: info@fdasolutionsgroup.com Phone: (305) 7023161

Related Public Records

Same Entity

Beautyxport s.r.o.

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 3043045982. Last updated year: 2026. Please use registration number 3043045982 when referencing this establishment in official correspondence.