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Data / Medical devices / Blood Pressure Cuff / United States

FDA-registered makers of Blood Pressure Cuff in the United States: 27 establishments

27 establishments in the United States are registered with the FDA to make Blood Pressure Cuff (product code DXQ). 20 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Blood Pressure Cuff
Product code
DXQ
Country
United States

Makers of Blood Pressure Cuff in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Welch Allyn, Inc.Skaneateles Falls, NY, United StatesManufacturer, Specification developer7December 16, 2025020api.fda.gov
American Diagnostic Corp.Hauppauge, NY, United StatesContract manufacturer, Manufacturer, Repackager or relabeler4May 15, 2015000api.fda.gov
Salter LabsEl Paso, TX, United StatesSpecification developer3December 19, 2008000api.fda.gov
Spacelabs Healthcare Inc.Snoqualmie, WA, United StatesManufacturer3October 27, 2015000api.fda.gov
D. E. Hokanson, Inc.Bellevue, WA, United StatesContract manufacturer, Manufacturer2August 6, 2004000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer2July 20, 1999000api.fda.gov
GE Medical Systems Information Technologies, Inc.Waukesha, WI, United StatesSpecification developer2April 9, 2013000api.fda.gov
GE Medical Systems Information Technologies, Inc.Wauwatosa, WI, United StatesSpecification developer2April 9, 2013010api.fda.gov
Med-Linket CorpAlhambra, CA, United StatesManufacturer2August 2, 2018000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer2June 13, 2016000api.fda.gov
Philips North America LLCCambridge, MA, United StatesComplaint file establishment, Specification developer2October 27, 2015000api.fda.gov
Suntech Medical, Inc.Morrisville, NC, United StatesManufacturer2October 20, 2008010api.fda.gov
Hosmed Inc.Doral, FL, United StatesManufacturer, Repackager or relabeler1October 28, 2009000api.fda.gov
Icu Medical, IncSalt Lake City, UT, United StatesManufacturer1May 5, 2016000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesSpecification developer1May 5, 2016020api.fda.gov
Koven Technology, Inc.Saint Louis, MO, United StatesManufacturer, Specification developer1April 14, 2015000api.fda.gov
LifeSync CorporationCoral Springs, FL, United StatesSpecification developer1March 20, 2007000api.fda.gov
Philips North America LLCAndover, MA, United StatesComplaint file establishment, Specification developer1December 20, 1990000api.fda.gov
Spiracle TechnologyLos Alamitos, CA, United StatesSpecification developer1January 13, 2005000api.fda.gov
Technicuff Corp.Leesburg, FL, United StatesManufacturer1September 6, 1994000api.fda.gov
A and D Engineering, Inc.Hoschton, GA, United StatesContract manufacturer0000api.fda.gov
Amarigo IncLos Angeles, CA, United StatesManufacturer0000api.fda.gov
Bound Tree Medical, LLCGrand Prairie, TX, United StatesManufacturer0000api.fda.gov
Dictum Health, Inc.Malibu, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Gregory MFG., Inc.Holyoke, MA, United StatesContract manufacturer0000api.fda.gov
Masimo CorporationIrvine, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
W.A. Baum Co., Inc.Copiague, NY, United StatesManufacturer, Repackager or relabeler0000api.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.