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Data / Medical devices / Flowmeter, Calibration, Gas

Flowmeter, Calibration, Gas (BXY): 25 FDA-registered makers in 8 countries

25 establishments in 8 countries are registered with the FDA to make Flowmeter, Calibration, Gas (product code BXY, Class 1, 21 CFR 868.2350). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 7 510(k) clearances under this code, the latest on September 15, 1995, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
BXY
Device class
1
Regulation
868.2350
Medical specialty
Anesthesiology

Makers by country

CountryMakers
United States11
China5
Mexico3
Taiwan2
Argentina1
Liechtenstein1
Switzerland1
Turkey1

Makers of Flowmeter, Calibration, Gas

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Allied Medical LLCEarth City, MO, United StatesManufacturer, Specification developer1February 21, 1986000api.fda.gov
Westmed Javid de Mexico, S.A. de C.V.NOGALES Sonora, MexicoManufacturer1September 15, 1995000api.fda.gov
Ameriflo2 IncorporatedIndianapolis, IN, United StatesManufacturer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Besmed Health Business CorporationNew Taipei City, TaiwanExporter to the US, Manufacturer0000api.fda.gov
Caire Inc.Ball Ground, GA, United StatesManufacturer0000api.fda.gov
Caire Inc.Ball Ground, GA, United StatesSpecification developer0000api.fda.gov
Create Biotech Co., Ltd.Taoyuan City, TaiwanManufacturer0000api.fda.gov
Danyang Airtech Co.,ltddanyang Jiangsu, ChinaManufacturer0000api.fda.gov
Danyang Xinya Valve Co., Ltd.Danyang Jiangsu, ChinaContract manufacturer, Manufacturer0000api.fda.gov
Ecleris SRLVilla Martelli Buenos Aires, ArgentinaManufacturer0000api.fda.gov
Flotec, Inc.Eagle Creek, IN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Fma Mechatronic Solutions AGSchaan, LiechtensteinContract manufacturer0000api.fda.gov
Foshan Kycare Medical Equipment Co. LtdFoshan City Guangdong, ChinaExporter to the US, Manufacturer0000api.fda.gov
Imt Analytics AGBuchs Sankt Gallen, SwitzerlandManufacturer0000api.fda.gov
IVEMSA S.A. de C.V DIVISION AG INDUSTRIESTijuana Baja California, MexicoManufacturer0000api.fda.gov
Jiangsu Jumao X-Care Medical Equipment Co., LtdDanyang Jiangsu, ChinaManufacturer0000api.fda.gov
Megasan Medikal Gaz Sistemleri Tibbi Alet Ve Cihazlar San. Tic. A. S.Cankiri, TurkeyManufacturer0000api.fda.gov
Netech Corp.E Farmingdale, NY, United StatesManufacturer0000api.fda.gov
Precision Fluidics Division Parker Hannifin Corp.Hatfield, PA, United StatesManufacturer0000api.fda.gov
Spiracle TechnologyLos Alamitos, CA, United StatesManufacturer0000api.fda.gov
Salaera, LLC d.b.a MaxtecSalt Lake City, UT, United StatesManufacturer0000api.fda.gov
Salter LabsEl Paso, TX, United StatesSpecification developer0000api.fda.gov
Salter Labs de Mexico de S.A. de C.V.Chihuahua Mexico, MexicoManufacturer0000api.fda.gov
Yuyao Jiahua Medical Appliance, Co., Ltd.Yuyao Zhejiang, ChinaManufacturer0000api.fda.gov

Updated September 15, 1995. 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.