Owen Mumford Limited

FDA Device Registration & Listing · Witney Oxfordshire, GB · Registration 3038110468

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
3038110468
FEI Number
3038110468
Entity Name
Owen Mumford Limited
City/State/Country
Witney Oxfordshire, GB
Establishment Address
De Havilland Way,, Witney Oxfordshire OX29 0YG, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
OWEN MUMFORD, LTD. (Owner Number: 8021764)
Owner / Operator Contact Address
Primsdown Industrial Estate, Chipping Norton, OXFORDSHIRE, GB-NOTA 0X7 5XP, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K210399
PMA Number
N/A

All Registered Proprietary Names

Unifine SafeControl Unifine Ultra

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2021-11-01

Official Correspondent

No official correspondent registered.

US Agent Details

TRAVIS SHAW Business: OWEN MUMFORD USA, INC. Email: travis.shaw@owenmumford.com Phone: (770) 9772226

Related Public Records

Same Entity

OWEN MUMFORD, LTD.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3003348846 Owen Mumford Limited Chipping Norton Oxfordshire, GB
8021764 OWEN MUMFORD, LTD. WOODSTOCK, OXFORDSHIRE, GB
3013143994 Owen Mumford Sdn Bhd Iskandar Puteri Johor, MY
1058602 OWEN MUMFORD USA, INC. MARIETTA, GA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038110468. Last updated year: 2026. Please use registration number 3038110468 when referencing this establishment in official correspondence.
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