Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010053755

FEI Number

3010053755

Entity Name

HAYMAX LIMITED

City/State/Country

Conwy Gwynedd, GB

Establishment Address

Unit 10a, Conwy Morfa Enterprise Park; Parc Caer Seion, Conwy Gwynedd LL32 8FA, GB

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

HayMax Limited (Owner Number: 10042550)

Owner / Operator Contact Address

Pharma Group, 10a Parc Caer Seion, Conwy, GB-CWY LL32 8FA, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K120894

PMA Number

N/A

All Registered Proprietary Names

HayMax Original HayMax Aloe Vera HayMax Lavender HayMax Pure

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	2012-12-07

Official Correspondent

Naomi Williams

US Agent Details

Danny West Business: FDA Agent Pro LLC Email: dwest@fdaagentpro.com Phone: (619) 4103383

Related Public Records

Same Entity

HayMax Limited

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 3010053755. Last updated year: 2026. Please use registration number 3010053755 when referencing this establishment in official correspondence.