MINTA MEDICAL LIMITED

FDA Device Registration & Listing · MERSEYSIDE Knowsley, GB · Registration 3004617090

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
3004617090
FEI Number
3004617090
Entity Name
MINTA MEDICAL LIMITED
City/State/Country
MERSEYSIDE Knowsley, GB
Establishment Address
CADDICK ROAD, MERSEYSIDE Knowsley L34 9HP, GB
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
MINTA MEDICAL LIMITED (Owner Number: 9064097)
Owner / Operator Contact Address
CADDICK ROAD, --, KNOWSLEY MERSEYSIDE, GB-NOTA L34 9HP, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

MINTA RYAN RF THERMOCOUPLE ELECTRODE NITINOL RADIOFREQUENCY LESION PROBE RADIOFREQUENCY THERMOCOUPLE ELECTRODE RADIOFREQUENCY ELECTRODE RF NITINOL THERMOCOUPLE ELECTRODE NITINOL RF ELECTRODE NITINOL REUSABLE RADIOFREQUENCY ELECTRODE DISPOSABLE RF THERMOCOUPLE ELECTRODE DISPOSABLE RF ELECTRODE RF ELECTRODE REUSABLE NITINOL RF ELECTRODE REUSABLE RADIOFREQUENCY ELECTRODE ADAPTER CABLE NITINOL REUSABLE RF ELECTRODE RADIO FREQUENCY LESION PROBE RADIO FREQUENCY THERMOCOUPLE ELECTRODE ADAPTER REUSABLE RF ELECTRODE RF ADAPTER CABLE RF THERMOCOUPLE ELECTRODE NITINOL RADIOFREQUENCY THERMOCOUPLE ELECTRODE NITINOL RADIOFREQUENCY ELECTRODE NITINOL RF THERMOCOUPLE ELECTRODE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GXI Probe, Radiofrequency Lesion Neurology Class 2 882.4725 2012-11-23

Official Correspondent

ANDREW EDWARDS

US Agent Details

PRESTON FRASIER Business: EPIMED INTERNATIONAL INC Email: PRESTONF@EPIMED.COM Phone: (518) 7250209

Related Public Records

Same Entity

MINTA MEDICAL LIMITED
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
K253907 ABBOTT MEDICAL Disposable Radiofrequency Cannula 2026-04-16
K242841 ABBOTT MEDICAL Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20) 2025-05-27

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0720-2020 Abbott Medical 2
CLASSIC Radiofrequency Cannula - Curved, 10 cm, SMK Compatible Electrode, REF C-1005-S - Product Usage: Disposable Radiofrequency Cannulae are provided in either straight, curved, or curved blunt geometries with a stylet inserted in the cannula. Cannulae are insulated except for the active tip. The active tip determines the size of the radiofrequency lesion.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004617090. Last updated year: 2026. Please use registration number 3004617090 when referencing this establishment in official correspondence.
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