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Data / Medical devices / Infusor, Pressure, For I.V. Bags / United States

FDA-registered makers of Infusor, Pressure, For I.V. Bags in the United States: 18 establishments

18 establishments in the United States are registered with the FDA to make Infusor, Pressure, For I.V. Bags (product code KZD). 1 has a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 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.

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Device
Infusor, Pressure, For I.V. Bags
Product code
KZD
Country
United States

Makers of Infusor, Pressure, For I.V. Bags in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Medical Solutions, Inc.Chantilly, VA, United StatesSpecification developer1October 29, 1997000api.fda.gov
ASP Global, LLCAustell, GA, United StatesSpecification developer0000api.fda.gov
CovidienLafayette, CO, United StatesSpecification developer0000api.fda.gov
Icu Medical, IncSalt Lake City, UT, United StatesManufacturer, Specification developer0000api.fda.gov
ICU Medical, Inc.Dublin, OH, United StatesManufacturer0000api.fda.gov
Mason Tayler Medical Products Corp.Buffalo, NY, United StatesSpecification developer0000api.fda.gov
Med-Linket CorpAlhambra, CA, United StatesManufacturer0000api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesSpecification developer0010api.fda.gov
Renu Medical, Inc.Everett, WA, United StatesComplaint file establishment, Repackager or relabeler, Reprocessor0000api.fda.gov
Solventum Us LLCEagan, MN, United StatesSpecification developer0000api.fda.gov
Salter LabsEl Paso, TX, United StatesSpecification developer0000api.fda.gov
Solventum US LLCSan Antonio, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Solventum US LLCEden Prairie, MN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Spacelabs Healthcare Inc.Snoqualmie, WA, United StatesManufacturer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
The Metrix CompanyDubuque, IA, United StatesContract manufacturer0000api.fda.gov
Transparent Supply Solutions Ltd.Dover, DE, United StatesSpecification developer0000api.fda.gov
TapmedicJacksonville, FL, United StatesSpecification developer0000api.fda.gov

Updated November 3, 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.