Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013438730

FEI Number

3013438730

Entity Name

MORGAN STEER ORTHOPAEDICS LTD

City/State/Country

Leicester Leicestershire, GB

Establishment Address

9 Furnace House, Narborough Wood Business Park, Desford Road, Enderby, Leicester Leicestershire LE19 4XT, GB

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Morgan Steer Orthopaedics Ltd (Owner Number: 10086241)

Owner / Operator Contact Address

9 Furnace House, Narborough Wood Business Park, Desford Road, Enderby, Leicester, GB-LEC LE19 4XT, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CIQ System Controller Cavity SpineWand Perc-D SpineWand KNS-1706-10 - Crawford 17 ga x 6 Cannula KNS-1904-10- DC 19 ga x 3 Cannula SCL600-01 - Crawford 17 ga x 6 cannula SCL800-01- Crawford 17 ga x 8 cannula

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2022-10-25
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2022-10-25
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2022-10-25
GEA	Cannula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2024-07-30

Official Correspondent

Matt Jelly

US Agent Details

Edwin Lindsay Business: RAF Solutions Inc Email: edwin@rafsolutions.net Phone: (305) 9607262

Related Public Records

Same Entity

Morgan Steer Orthopaedics 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
K970809	Somnus Medical Technologies, Inc.	BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL	1997-06-18
K222793	C.R. Bard, Inc.	WavelinQ Generator	2022-10-17
K002257	Tecno Instruments (Pvt.) , Ltd.	TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100	2000-10-19
K193591	Bowa-Electronics GmbH & Co. KG	ARC 400	2020-04-02
K192128	Sutter Medizintechnik GmbH	Sutter Arrowtip Monopolar Electrodes	2019-10-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-06	Rita Medical Systems	2	Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

Similar Registrations

Registration Number	Establishment Name	Location
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3020623326	TRIWORKS GROUP S.R.L.	Palata Campobasso, IT
3012616488	BRERA MEDICAL INCORPORATED	Northborough, MA, US
3012940012	Sutter Medical Technologies USA Inc.	Alpharetta, GA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013438730. Last updated year: 2026. Please use registration number 3013438730 when referencing this establishment in official correspondence.