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Medical Wire And Equipment Co. Ltd.: FDA-registered device maker in Corsham, Wiltshire, United Kingdom, 2 510(k) clearances

Name: Medical Wire And Equipment Co. Ltd. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Medical Wire And Equipment Co. Ltd. is registered with the FDA (registration 9610649) in Corsham, Wiltshire, United Kingdom. It lists 16 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 30, 2008. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number: 9610649
FEI number: 3002807578
Address: Potley, Corsham, Wiltshire, United Kingdom, SN13 9RT
Owner or operator: MEDICAL WIRE AND EQUIPMENT CO. LTD. (8021919)
Roles: Manufacturer
First device listed: November 13, 1992
Registered through: 2026
Brand names listed: Amnicator, Applicator, Collector, Culture Medium, Dry Swab, Isolation Supplements, Micro Loops, Microring (Except for YT) and more

Devices it lists

Device	Product code	Class	Role	Source
Applicator, Absorbent Tipped, Non-Sterile	KXF	1	Manufacturer	accessdata.fda.gov
Applicator, Absorbent Tipped, Sterile	KXG	1	Manufacturer	accessdata.fda.gov
Applicator, Ent	KCJ	1	Manufacturer	accessdata.fda.gov
Container, Specimen, Sterile	FMH	1	Manufacturer	accessdata.fda.gov
Culture Media, Anaerobic Transport	JSL	1	Manufacturer	accessdata.fda.gov
Culture Media, Non-Propagating Transport	JSM	1	Manufacturer	accessdata.fda.gov
Culture Media, Selective And Differential	JSI	1	Manufacturer	accessdata.fda.gov
Culture Media, Selective And Non-Differential	JSJ	1	Manufacturer	accessdata.fda.gov
Device, General Purpose, Microbiology, Diagnostic	LIB	1	Manufacturer	accessdata.fda.gov
Device, Specimen Collection	LIO	1	Manufacturer	accessdata.fda.gov
Discs, Strips And Reagents, Microorganism Differentiation	JTO	1	Manufacturer	accessdata.fda.gov
Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	LXG	1	Manufacturer	accessdata.fda.gov
Kit, Identification, Yeast	JXB	1	Manufacturer	accessdata.fda.gov
Kit, Quality Control For Culture Media	JTR	1	Manufacturer	accessdata.fda.gov
Sampler, Amniotic Fluid (Amniocentesis Tray)	HIO	1	Manufacturer	accessdata.fda.gov
Supplement, Culture Media	JSK	1	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
December 30, 2008	K082472	VIROCULT, MODEL MW950	LIO	Substantially Equivalent	Medical Wire & Equipment Company (Bath), Ltd.	accessdata.fda.gov
June 23, 1987	K872213	TRANSTUBE MW176 OT MD176	JSM	Substantially Equivalent	Medical Wire & Equipment Co.	accessdata.fda.gov

Compare with other makers

Updated December 30, 2008. 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.