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Data / Medical devices / Tracheostomy And Nasal Suctioning Kit

Tracheostomy And Nasal Suctioning Kit (LRQ): 9 FDA-registered makers in 3 countries

9 establishments in 3 countries are registered with the FDA to make Tracheostomy And Nasal Suctioning Kit (product code LRQ, Class 1). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 6 510(k) clearances under this code, the latest on November 27, 1996, and lists 2 recall events (1 Class I). FDA data exported November 2, 2026.

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Product code
LRQ
Device class
1
Medical specialty
Unknown

Makers by country

CountryMakers
China4
United States3
Mexico2

Makers of Tracheostomy And Nasal Suctioning Kit

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
Allmed Medical Products Co., Ltd.Zhijiang City Hubei, ChinaContract manufacturer0000api.fda.gov
Allmed Medical Products Co., Ltd.ZHIJIANG CITY Hubei, ChinaContract manufacturer0000api.fda.gov
Centurion Medical Products, LPHowell, MI, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Cardinal Health 200, LLCEl Paso, TX, United StatesManufacturer0000api.fda.gov
Convertors de Mexico S. de R.L. de C.VCD.JUAREZ Chihuahua, MexicoManufacturer0000api.fda.gov
Dukal LLCRonkonkoma, NY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Hangzhou Primecare Medical Co.,Ltd.hangzhou Zhejiang, ChinaExporter to the US, Manufacturer0000api.fda.gov
Primecare Medical (Suzhou) Co.,Ltd.Changshu Jiangsu, ChinaContract manufacturer0000api.fda.gov
Tri-State De Mexico, S. De R.L. De C.V.MEXICALI Baja California, MexicoManufacturer, Repackager or relabeler0000api.fda.gov

Updated November 27, 1996. 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.