Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3045079085

FEI Number

3045079085

Entity Name

XIALLA

City/State/Country

Ottawa Ontario, CA

Establishment Address

57 Wilton Crescent, Ottawa Ontario K1S 2T6, CA

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Xialla (Owner Number: 10095660)

Owner / Operator Contact Address

57 Wilton Crescent, Ottawa, CA-ON K1S 2T6, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Xialla Adhesive Pads Xialla Kit Xialla Device

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LKY	Device, External Penile Rigidity	Gastroenterology, Urology	Class 2	876.5020	2026-04-09

Official Correspondent

Nigel Shaw

US Agent Details

David Readman Email: dave.readman@gmail.com Phone: (858) 7358488

Related Public Records

Same Entity

Xialla

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 3045079085. Last updated year: 2026. Please use registration number 3045079085 when referencing this establishment in official correspondence.