Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010170586

FEI Number

3010170586

Entity Name

MERIDIAN MEDICAL LIMITED

City/State/Country

Littlehampton West Sussex, GB

Establishment Address

Unit 1, Thorgate Road, Lineside Industrial Estate, Littlehampton West Sussex BN17 7LU, GB

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Meridian Medical Limited (Owner Number: 10042404)

Owner / Operator Contact Address

Unit 1, Thorgate Road, Lineside Industrial Estate, Littlehampton, GB-WSX BN17 7LU, GB

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Carilex Medical, Inc. LIDCO mosaic

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSO	Catheter, Conduction, Anesthetic	Anesthesiology	Class 2	868.5120	2012-11-28
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2018-12-20
KLA	Monitor, Esophageal Motility, Anorectal Motility, And Tube	Gastroenterology, Urology	Class 2	876.1725	2012-11-28
KGZ	Accessories, Catheter	General, Plastic Surgery	Class 1	878.4200	2012-11-23
FWZ	Operating Room Accessories Table Tray	General, Plastic Surgery	Class 1	878.4950	2012-11-28
DXG	Computer, Diagnostic, Pre-Programmed, Single-Function	Cardiovascular	Class 2	870.1435	2020-12-03
JDG	Prosthesis, Hip, Femoral Component, Cemented, Metal	Orthopedic	Class 2	888.3360	2012-11-28
FFO	Retractor, Self-Retaining	Gastroenterology, Urology	Class 1	876.4730	2020-12-03

Official Correspondent

Andrew Wootten

US Agent Details

Matt Dryden Business: Estrin Consulting Group LLC Email: matt.dryden@promedic.cc Phone: (239) 3076063

Related Public Records

Same Entity

Meridian 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
K072702	Stryker Instruments, Instruments Div.	STRYKER ANTIMIC CATHETER	2008-03-19
K780497	American Ortomed Corp.	SPHERISTEM TOTAL HIP PROSTHESIS	1978-06-14

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9680425	Avent S. de R.L. de C.V.	TIJUANA Baja California, MX
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010170586. Last updated year: 2026. Please use registration number 3010170586 when referencing this establishment in official correspondence.