ODSTOCK MEDICAL LTD

FDA Device Registration & Listing · SALISBURY Wiltshire, GB · Registration 3005344585

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
3005344585
FEI Number
3005344585
Entity Name
ODSTOCK MEDICAL LTD
City/State/Country
SALISBURY Wiltshire, GB
Establishment Address
SALISBURY DISTRICT HOSPITAL, National Clinical FES Centre, SALISBURY Wiltshire SP2 8BJ, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
ODSTOCK MEDICAL LTD (Owner Number: 9076759)
Owner / Operator Contact Address
SALISBURY DISTRICT HOSPITAL, --, SALISBURY, GB-WIL SP2 8BJ, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K171396
PMA Number
N/A

All Registered Proprietary Names

ODFS Pace XL

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZI Stimulator, Neuromuscular, External Functional Neurology Class 2 882.5810 2018-06-29
IPF Stimulator, Muscle, Powered Physical Medicine Class 2 890.5850 2018-06-29

Official Correspondent

No official correspondent registered.

US Agent Details

Gary VILES Business: Neuro Rehab Recovery Inc Email: innovmedical@gmail.com Phone: (813) 4350772

Related Public Records

Same Entity

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

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K030403 Cefar Medical AB CEFAR REHAB 2 AND REHAB 2 PRO 2003-07-17
K231440 Shenzhen Roundwhale Technology Co. , Ltd. Combo Electrotherapy Device 2023-11-03
K820884 Nitron Electronics ELECTRICAL MUSCLE STIMULATOR 1982-04-29
K201958 Therasigma, LLC ETD Family of Electrotherapy Devices 2020-08-04
K964028 Mettler Electronics Corp. SYS STIM 226 1997-02-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005344585. Last updated year: 2026. Please use registration number 3005344585 when referencing this establishment in official correspondence.
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