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Data / Medical devices / Paracentesis Tray

Paracentesis Tray (PYC): 5 FDA-registered makers in 3 countries

5 establishments in 3 countries are registered with the FDA to make Paracentesis Tray (product code PYC, Class 1, 21 CFR 878.4200). 0 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 3 recall events (1 Class I). FDA data exported November 2, 2026.

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Product code
PYC
Device class
1
Regulation
878.4200
Medical specialty
General, Plastic Surgery

Makers by country

CountryMakers
United States3
China1
Mexico1

Makers of Paracentesis Tray

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
Cardinal Health 200, LLCEl Paso, TX, United StatesManufacturer0000api.fda.gov
Changzhou CareU Medical Instruments Co., Ltd.Changzhou City Jiangsu, ChinaManufacturer0000api.fda.gov
Convertors de Mexico S. de R.L. de C.VCD.JUAREZ Chihuahua, MexicoManufacturer, Repackager or relabeler0000api.fda.gov
Merit Medical Systems, IncChester, VA, United StatesContract manufacturer0000api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesManufacturer0010api.fda.gov

Updated November 2, 2026. 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.