Data / Medical devices / Monitor, St Segment With Alarm / United States

FDA-registered makers of Monitor, St Segment With Alarm in the United States: 21 establishments

Name: FDA-registered makers of Monitor, St Segment With Alarm in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

21 establishments in the United States are registered with the FDA to make Monitor, St Segment With Alarm (product code MLD). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device: Monitor, St Segment With Alarm
Product code: MLD
Country: United States

Makers of Monitor, St Segment With Alarm in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Source
Criticare Technologies, Inc.	Warwick, RI, United States	Manufacturer, Repackager or relabeler	1	September 1, 2010	api.fda.gov
Advanced Instrumentations, Inc.	Miami, FL, United States	Manufacturer	0		api.fda.gov
Athena GTX	Johnston, IA, United States	Complaint file establishment, Manufacturer	0		api.fda.gov
Caf Medical Solutions Inc	Hockley, TX, United States	Manufacturer	0		api.fda.gov
CDR Manufacturing, Inc., DBA Keytronic	Oakdale, MN, United States	Contract manufacturer	0		api.fda.gov
Draeger Medical Systems, Inc.	Andover, MA, United States	Complaint file establishment, Manufacturer	0		api.fda.gov
EDAN Diagnostics, Inc.	San Diego, CA, United States	Contract manufacturer	0		api.fda.gov
Engineered Medical Systems, LLC	Bartlett, TN, United States	Contract manufacturer	0		api.fda.gov
Ge Medical Systems Information Technologies	El Paso, TX, United States	Manufacturer, Repackager or relabeler	0		api.fda.gov
GE Medical Systems Information Technologies, Inc.	Waukesha, WI, United States	Specification developer	0		api.fda.gov
GE Medical Systems Information Technologies, Inc.	Wauwatosa, WI, United States	Specification developer	0		api.fda.gov
Hosmed Inc.	Doral, FL, United States	Manufacturer, Repackager or relabeler	0		api.fda.gov
MINDRAY DS USA, Inc.	Mahwah, NJ, United States	Complaint file establishment, Contract manufacturer	0		api.fda.gov
Philips North America LLC	Cambridge, MA, United States	Complaint file establishment, Specification developer	0		api.fda.gov
Philips North America LLC	Andover, MA, United States	Manufacturer, Specification developer	0		api.fda.gov
Philips North America LLC	Murrysville, PA, United States	Contract manufacturer	0		api.fda.gov
Philips North America LLC	Export, PA, United States	Contract manufacturer	0		api.fda.gov
Repair Operations Center	Oak Creek, WI, United States	Remanufacturer	0		api.fda.gov
Spacelabs Healthcare Inc.	Snoqualmie, WA, United States	Manufacturer	0		api.fda.gov
VectraCor, Inc.	Totowa, NJ, United States	Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer	0		api.fda.gov
Welch Allyn, Inc.	Skaneateles Falls, NY, United States	Specification developer	0		api.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.