REXYN LTD

FDA Device Registration & Listing · Prescot Liverpool, GB · Registration 3010030809

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
3010030809
FEI Number
3010030809
Entity Name
REXYN LTD
City/State/Country
Prescot Liverpool, GB
Establishment Address
11 Kensington Drive, Prescot Liverpool L34 1WD, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Rexyn Ltd (Owner Number: 10083472)
Owner / Operator Contact Address
P O Box 226, Prescot, GB-LIV L34 1WD, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Airpod ATM-Airpod Easy Applicator MultiBoard Easy Applicator

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QGI Air-Handling Apparatus Accessory General, Plastic Surgery Class 1 878.5080 2021-11-23
FPS Board, Bed General Hospital Class 1 880.6070 2021-11-23
FMR Device, Transfer, Patient, Manual General Hospital Class 1 880.6785 2021-11-23

Official Correspondent

Yogen Jasani Jasani

US Agent Details

Emily Matorin Business: FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Rexyn Ltd
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Similar Registrations

Registration Number Establishment Name Location
3018094310 Medtronic Engineering and Innovation Center (MEIC) Hyderabad Telangana, IN
3008493151 SurgiSmoke Solutions Saint Paul, MN, US
3026612481 Covidien Lafayette, CO, US
1450662 Isomedix Operations, Inc. Libertyville, IL, US
3015967359 Stryker Instruments Portage, MI, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010030809. Last updated year: 2026. Please use registration number 3010030809 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.