Data / Medical devices / United Kingdom / GVS Filter Technology UK Ltd

GVS Filter Technology UK Ltd: FDA-registered device maker in Lancaster Lancashire, United Kingdom, 3 510(k) clearances

Name: GVS Filter Technology UK Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

GVS Filter Technology UK Ltd is registered with the FDA (registration 3004428458) in Lancaster Lancashire, United Kingdom. It lists 12 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 1, 2005. Registered through 2027. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch GVS Filter Technology UK Ltd

FDA registration number: 3004428458
Address: Caton Road, Lancaster Lancashire, United Kingdom, LA1 3PE
Owner or operator: GVS Filter Technology UK Ltd. (9098065)
Roles: Contract manufacturer, Manufacturer, Specification developer
First device listed: February 26, 2007
Registered through: 2027
Brand names listed: 100, 1420, 1460/05, 1460/06, 1600, 2000, 2200/47BDKBTUA123/0001, 2200/48BIKBTUA123/0001 and more

Devices it lists

Device	Product code	Class	Role	Source
Accessory To Continuous Ventilator (Respirator)	MOD	2	Manufacturer, Specification developer	accessdata.fda.gov
Clip, Nose	BXJ	1	Manufacturer	accessdata.fda.gov
Condenser, Heat And Moisture (Artificial Nose)	BYD	1	Manufacturer, Specification developer	accessdata.fda.gov
Continuous, Minimal Ventilatory Support, Facility Use Ventilator	MNT	2	Contract manufacturer	accessdata.fda.gov
Continuous, Ventilator, Home Use	NOU	2	Contract manufacturer	accessdata.fda.gov
Filter, Bacterial, Breathing-Circuit	CAH	2	Manufacturer, Specification developer	accessdata.fda.gov
Spirometer, Diagnostic	BZG	2	Manufacturer, Specification developer	accessdata.fda.gov
Tube, Smoke Removal, Endoscopic	FCZ	1	Manufacturer	accessdata.fda.gov
Tubing/Tubing With Filter, Insufflation, Laparoscopic	NKC	1	Manufacturer	accessdata.fda.gov
Ventilator, Continuous, Facility Use	CBK	2	Contract manufacturer	accessdata.fda.gov
Ventilator, Non-Continuous (Respirator)	BZD	2	Contract manufacturer	accessdata.fda.gov
Ventilatory Effort Recorder	MNR	2	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
September 1, 2005	K051712	MODEL 2800 PFT FILTER	BZG	Substantially Equivalent	Air Safety, Ltd.	accessdata.fda.gov
June 3, 2004	K040712	AIR SAFETY HEPA, MODEL 3500	MOD	Substantially Equivalent	Air Safety, Ltd.	accessdata.fda.gov
May 13, 2004	K033008	AIR SAFETY HEPA AND NON-HEPA FILTERS	CAH	Substantially Equivalent	Air Safety, Ltd.	accessdata.fda.gov

Compare with other makers

Updated September 1, 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.