Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023190433

FEI Number

3023190433

Entity Name

CARDIOPRECISION LTD

City/State/Country

Glasgow Lancashire, GB

Establishment Address

Innovation Centre, 1 Ainslie Road, Hillington, Glasgow Lancashire G52 4RU, GB

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

CardioPrecision Ltd (Owner Number: 10085327)

Owner / Operator Contact Address

Innovation Centre, 1 Ainslie Road, Hillington, Glasgow, GB-RFW G52 4RU, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CoreVista® Retractor CoreVista® Retractor System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DWS	Instruments, Surgical, Cardiovascular	Cardiovascular	Class 1	870.4500	2022-06-03

Official Correspondent

Ying Sutherland

US Agent Details

Keith Lambie Business: State of the Art Medical Products, Inc. Email: KLambie@sotamedical.com Phone: (973) 5712400

Related Public Records

Same Entity

CardioPrecision Ltd

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0008-04	Rultract Inc	1	Rultract Surgical Retractor, 4100 Series, all system configurations, reusable.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023190433. Last updated year: 2026. Please use registration number 3023190433 when referencing this establishment in official correspondence.