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Data / Medical devices / Transducer, Gas Flow

Transducer, Gas Flow (BXP): 17 FDA-registered makers in 6 countries

17 establishments in 6 countries are registered with the FDA to make Transducer, Gas Flow (product code BXP, Class 1, 21 CFR 868.2885). 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 March 31, 1994, and lists 0 recall events (0 Class I). 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 every maker of this deviceMakers in the United StatesWatch this device
Product code
BXP
Device class
1
Regulation
868.2885
Medical specialty
Anesthesiology

Makers by country

CountryMakers
United States6
Germany6
Taiwan2
Switzerland1
Israel1
Brazil1

Makers of Transducer, Gas Flow

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 StatesManufacturer1March 16, 1977000api.fda.gov
Unipower Corp.Minnetonka, MN, United StatesManufacturer1March 31, 1994000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Besmed Health Business CorporationNew Taipei City, TaiwanManufacturer0000api.fda.gov
Create Biotech Co., Ltd.Taoyuan City, TaiwanManufacturer0000api.fda.gov
Draeger Medical Systems, Inc.Andover, MA, United StatesManufacturer0000api.fda.gov
Draeger Interservices GmbHLuebeck Schleswig-Holstein, GermanyContract manufacturer0000api.fda.gov
Draegerwerk AG & Co. KGaALUEBECK Schleswig-Holstein, GermanyManufacturer0000api.fda.gov
Englert GMBH & Co. KGWertheim Baden-Wurttemberg, GermanyContract manufacturer0000api.fda.gov
Honeywell Healthcare Solutions GmbH (formerly EnviteC)WISMAR Mecklenburg-Western Pomerania, GermanyContract manufacturer, Manufacturer0000api.fda.gov
Jaeger Medical GmbHHOECHBERG Bavaria, GermanyComplaint file establishment, Specification developer0000api.fda.gov
NDD Medizintechnik AGZurich, SwitzerlandComplaint file establishment, Specification developer0000api.fda.gov
Peak Medical Ltd.Netanya Central, IsraelSpecification developer0000api.fda.gov
Philips Medical Systems LtdaVarginha Minas Gerais, BrazilSpecification developer0000api.fda.gov
Respironics Novametrix, LLCAndover, MA, United StatesSpecification developer0000api.fda.gov
Sensatronic GMBHWismar Mecklenburg-Western Pomerania, GermanyManufacturer0000api.fda.gov
Zoll Medical CorporationChelmsford, MA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov

Updated March 31, 1994. 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.