PODOPRO UK LTD

FDA Device Registration & Listing · HUDDERSFIELD England, GB · Registration 3010615336

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
3010615336
FEI Number
3010615336
Entity Name
PODOPRO UK LTD
City/State/Country
HUDDERSFIELD England, GB
Establishment Address
Riverside Court, Stoney Battery Road, HUDDERSFIELD England HD1 4TW, GB
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer),Foreign Private Label Distributor,Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Podopro UK Ltd (Owner Number: 10046445)
Owner / Operator Contact Address
Riverside Court, Huddersfield, GB-ENG HD1 4TW, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pedinol

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2014-03-24

Official Correspondent

No official correspondent registered.

US Agent Details

Susan Spillaine Business: Sonic Packaging Email: susan@sonicpackaging.com Phone: (201) 6664744

Related Public Records

Same Entity

Podopro UK 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 3010615336. Last updated year: 2026. Please use registration number 3010615336 when referencing this establishment in official correspondence.
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