Data / Medical devices / United Kingdom / Meridian Medical Limited

Meridian Medical Limited: FDA-registered device maker in Littlehampton West Sussex, United Kingdom, 3 510(k) clearances

Name: Meridian Medical Limited FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Meridian Medical Limited is registered with the FDA (registration 3010170586) in Littlehampton West Sussex, United Kingdom. It lists 12 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 7, 2005. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3010170586
Address: Unit 1, Thorgate Road Lineside Industrial Estate, Littlehampton West Sussex, United Kingdom, BN17 7LU
Owner or operator: Meridian Medical Limited (10042404)
Roles: Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed: November 23, 2012
Registered through: 2026
Brand names listed: Carilex Medical, Carilex Medical, Inc., LIDCO, mosaic

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Catheter	KGZ	1	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Apparatus, Suction, Operating-Room, Wall Vacuum Powered	GCX	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Catheter, Conduction, Anesthetic	BSO	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Computer, Diagnostic, Pre-Programmed, Single-Function	DXG	2	Contract manufacturer	accessdata.fda.gov
Device, Cystometric, Hydraulic	FEN	2	Contract manufacturer, Repackager or relabeler	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Contract manufacturer	accessdata.fda.gov
Monitor, Esophageal Motility, Anorectal Motility, And Tube	KLA	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Negative Pressure Wound Therapy Powered Suction Pump	OMP	2	Contract manufacturer	accessdata.fda.gov
Operating Room Accessories Table Tray	FWZ	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Probe And Director, Gastro-Urology	FGM	1	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Prosthesis, Hip, Femoral Component, Cemented, Metal	JDG	2	Manufacturer, Repackager or relabeler	accessdata.fda.gov
Retractor, Self-Retaining	FFO	1	Contract manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
July 7, 2005	K051524	LOCK-IT PLUS REGIONAL ANESTHESIA CATHETER SECUREMENT DEVICE, MODEL 100/399/216	BSO	Substantially Equivalent	Smiths Medical Asd, Inc.	accessdata.fda.gov
January 16, 2004	K031617	MEDIPLUS SINGLE USE LOWER GI MANOMETRY CATHETER	KLA	Substantially Equivalent	Mediplus , Ltd.	accessdata.fda.gov
November 10, 1999	K992234	THE TAPER-FIT TOTAL HIP SYSTEM	JDG	Substantially Equivalent	Corin USA	accessdata.fda.gov

Compare with other makers

Updated July 7, 2005. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.