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Data / Medical devices / Transducer, Gas Pressure, Differential

Transducer, Gas Pressure, Differential (BYR): 4 FDA-registered makers in 3 countries

4 establishments in 3 countries are registered with the FDA to make Transducer, Gas Pressure, Differential (product code BYR, Class 1, 21 CFR 868.2875). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 3 510(k) clearances under this code, the latest on February 22, 1990, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
BYR
Device class
1
Regulation
868.2875
Medical specialty
Anesthesiology

Makers by country

CountryMakers
United States2
Taiwan1
China1

Makers of Transducer, Gas Pressure, Differential

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
Create Biotech Co., Ltd.Taoyuan City, TaiwanManufacturer0000api.fda.gov
Enercon TechnologiesGray, ME, United StatesContract manufacturer0000api.fda.gov
Mannkind CorporationDanbury, CT, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Zhangjiagang Carenovo Technology Co., Ltd.Zhangjiagang Jiangsu, ChinaManufacturer0000api.fda.gov

Updated February 22, 1990. 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.