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Data / Medical devices / Computer, Oxygen-Uptake / United States

FDA-registered makers of Computer, Oxygen-Uptake in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Computer, Oxygen-Uptake (product code BZL). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Computer, Oxygen-Uptake
Product code
BZL
Country
United States

Makers of Computer, Oxygen-Uptake in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aei Technologies Inc.Bastrop, TX, United StatesManufacturer2April 8, 1993000api.fda.gov
Medical Graphics Corp.Saint Paul, MN, United StatesManufacturer2April 16, 2007000api.fda.gov
Korr Medical Technologies, Inc.Salt Lake City, UT, United StatesManufacturer1January 2, 2003000api.fda.gov
TF Health Corp.Phoenix, AZ, United StatesComplaint file establishment, Repackager or relabeler, Specification developer1September 25, 2020000api.fda.gov
Vacumed, Div. Of Vacumetrics, Inc.Ventura, CA, United StatesManufacturer1March 4, 1987000api.fda.gov
Medipines CorporationYorba Linda, CA, United StatesManufacturer, Specification developer0000api.fda.gov
Repair Operations CenterOak Creek, WI, United StatesRemanufacturer0000api.fda.gov
TreyMed, Inc.Sussex, WI, United StatesContract manufacturer0000api.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.