Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011788145

FEI Number

3011788145

Entity Name

Nasaleze Group

City/State/Country

Douglas, IM

Establishment Address

Unit 3 Woodside House, Ballafletcher Business Park, Douglas IM44QE, IM

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Nasaleze International Ltd (Owner Number: 10049830)

Owner / Operator Contact Address

Euromanx House, Freeport, Ballasalla, IM-NOTA IM9 2AP, IM

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K132520

PMA Number

N/A

All Registered Proprietary Names

AllerBlock Junior Alzair AllerBlock Adult AllerBlock Travel

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUP	Cream, Nasal, Topical, Mechanical Allergen Particle Barrier	General Hospital	Class 2	880.5045	2021-12-15
NUP	Cream, Nasal, Topical, Mechanical Allergen Particle Barrier	General Hospital	Class 2	880.5045	2017-06-20
NUP	Cream, Nasal, Topical, Mechanical Allergen Particle Barrier	General Hospital	Class 2	880.5045	2015-08-07

Official Correspondent

Matt Duxbury

US Agent Details

Dennis Moore Business: Auk Technical Services LLC Email: dm@aukts.com Phone: (916) 3005319

Related Public Records

Same Entity

Nasaleze International 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 3011788145. Last updated year: 2026. Please use registration number 3011788145 when referencing this establishment in official correspondence.