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Data / Medical devices / Container, Specimen, Urine, Drugs Of Abuse, Over The Counter

Container, Specimen, Urine, Drugs Of Abuse, Over The Counter (MPQ): 20 FDA-registered makers in 7 countries

20 establishments in 7 countries are registered with the FDA to make Container, Specimen, Urine, Drugs Of Abuse, Over The Counter (product code MPQ, Class 1, 21 CFR 864.3260). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, 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.

Product code
MPQ
Device class
1
Regulation
864.3260
Medical specialty
Pathology

Makers by country

CountryMakers
United States10
China5
Switzerland1
Egypt1
Thailand1
India1
Indonesia1

Makers of Container, Specimen, Urine, Drugs Of Abuse, Over The Counter

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
American Plastics Co., Inc.Glendale, AZ, United StatesContract manufacturer0000api.fda.gov
Berlinger Special AGGanterschwil Sankt Gallen, SwitzerlandManufacturer0000api.fda.gov
Biomedical Polymers, Inc.Sterling, MA, United StatesManufacturer0000api.fda.gov
Diatrust Medical Co., Ltd.Nanjing City Jiangsu, ChinaManufacturer0000api.fda.gov
Diagnostic Automation/ Cortez Diagnostics Inc,.Woodland Hills, CA, United StatesManufacturer0000api.fda.gov
Elhoda Trade And SuppliesBadr industerial city Al Qahirah, EgyptManufacturer0000api.fda.gov
Home Richfull Technology (thailand) Company LimitedBan Khai Rayong, ThailandManufacturer0000api.fda.gov
Hynaut Health Technology Co., LTD.Qingdao Shandong, ChinaContract manufacturer, Manufacturer0000api.fda.gov
ICON Injection Molding, Inc.Phoenix, AZ, United StatesContract manufacturer, Manufacturer0000api.fda.gov
K-Med Co., Ltd.Yangzhou Jiangsu, ChinaManufacturer0000api.fda.gov
Mallinckrodt Manufacturing LLCMadison, WI, United StatesManufacturer, Remanufacturer0000api.fda.gov
Narang Medical, Ltd.New Delhi, IndiaManufacturer0000api.fda.gov
Omega Laboratories, Inc.Mogadore, OH, United StatesSpecification developer0000api.fda.gov
Packaging Compliance Medical, LLCKentwood, MI, United StatesContract manufacturer0000api.fda.gov
Phamatech Inc.San Diego, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
PT. Jayamas Medica Industri TbkSidoarjo Jawa Timur, IndonesiaContract manufacturer0000api.fda.gov
Therapak, LLCOakwood, GA, United StatesManufacturer0000api.fda.gov
Therapak, LLCClaremont, CA, United StatesManufacturer0000api.fda.gov
Xiamen Aquatown Technology Co., LtdXiamen Fujian, ChinaManufacturer0000api.fda.gov
Zhejiang Sorfa Life Science Research Co., Ltd.Hangzhou Zhejiang, ChinaExporter to the US, Manufacturer0000api.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.