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Data / Medical devices / Plethysmograph, Impedance / United States

FDA-registered makers of Plethysmograph, Impedance in the United States: 27 establishments

27 establishments in the United States are registered with the FDA to make Plethysmograph, Impedance (product code DSB). 8 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
Plethysmograph, Impedance
Product code
DSB
Country
United States

Makers of Plethysmograph, Impedance in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Seemedx, IncLas Vegas, NV, United StatesSpecification developer5January 22, 2014000api.fda.gov
Innovamed Sphere IncFall River, MA, United StatesComplaint file establishment, Specification developer2June 18, 2009000api.fda.gov
Aci Medical, LLCSan Marcos, CA, United StatesManufacturer1October 14, 1988000api.fda.gov
Bodyport Inc.San Francisco, CA, United StatesComplaint file establishment, Specification developer1July 29, 2022000api.fda.gov
D. E. Hokanson, Inc.Bellevue, WA, United StatesManufacturer1January 18, 1990000api.fda.gov
Fujifilm Sonosite,inc.Bothell, WA, United StatesRemanufacturer1June 3, 2011000api.fda.gov
Impedimed, Inc.Carlsbad, CA, United StatesSpecification developer1October 17, 2023000api.fda.gov
Valhalla Scientific, Inc.Poway, CA, United StatesManufacturer1January 5, 1987000api.fda.gov
Acist Medical Systems, Inc.Eden Prairie, MN, United StatesComplaint file establishment, Contract manufacturer0000api.fda.gov
Analog DevicesWilmington, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Becton, Dickinson And CompanyIrvine, CA, United StatesSpecification developer0000api.fda.gov
Benchmark Electronics, Inc.Winona, MN, United StatesContract manufacturer0000api.fda.gov
Caf Medical Solutions IncHockley, TX, United StatesManufacturer0000api.fda.gov
CDR Manufacturing, Inc., DBA KeytronicOakdale, MN, United StatesContract manufacturer0000api.fda.gov
Draeger Medical Systems, Inc.Andover, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
EDAN Diagnostics, Inc.San Diego, CA, United StatesContract manufacturer0000api.fda.gov
Edwards Lifesciences Technology SarlAnasco, PR, United StatesManufacturer0000api.fda.gov
Graphic Controls Acquisition Corp.dba Nissha Medical TechnologiesBuffalo, NY, United StatesContract manufacturer0000api.fda.gov
Hosmed Inc.Doral, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
MINDRAY DS USA, Inc.Mahwah, NJ, United StatesComplaint file establishment, Contract manufacturer0000api.fda.gov
Millstone Medical Outsourcing LLCOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov
NextPhase Medical Devices, LLCMansfield, MA, United StatesContract manufacturer0000api.fda.gov
OnCore ManufacturingWestborough, MA, United StatesContract manufacturer0000api.fda.gov
Respironics Novametrix, LLCAndover, MA, United StatesSpecification developer0000api.fda.gov
SwemcoMoorestown, NJ, United StatesContract manufacturer0000api.fda.gov
Welch Allyn, Inc.Skaneateles Falls, NY, United StatesSpecification developer0000api.fda.gov
ZOLL Manufacturing CorporationPittsburgh, PA, United StatesManufacturer0000api.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.