Vapotherm Inc. is a publicly held corporation based in Exeter, New Hampshire that was founded in 1999 as a medical device manufacturer after creating the first heated and humidified high flow therapy nasal cannula system.

Vapotherm, Inc.
Company typePublic
OTCQXVAPO (since 2023)
NYSE: VAPO
IndustryMedical devices
FoundedJanuary 1, 1999 (1999-01-01) in Stevensville, MD, U.S.
FoundersBill Niland
Jun Cortez
HeadquartersExeter, New Hampshire, U.S
Area served
Worldwide
Brands
  • HVT 2.0®
  • Precision Flow®
  • Precision Flow Heliox®
  • Flowrest®
Number of employees
116 (2015)
Websitevapotherm.com Edit this at Wikidata

Vapotherm Precision Flow

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In 2009, Vapotherm released a new flagship product replacing the Vapotherm 2000i (that had been recalled in 2005, and then re-approved for use in the market in 2006); boasting a completely integrated electronic flow meter and electronic blender, as well as an internal oxygen analyzer. The Precision Flow is currently Vapotherm's flagship capital unit and is the premier medical device for providing high flow therapy.

Precision Flow Heliox

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Through an agreement with Praxair, Vapotherm provides a Precision Flow model specially calibrated specifically for 80:20 heliox gas for use in patients who may benefit from heliox therapy.

Vapotherm Q50 Compressor

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In November 2015 Vapotherm announced its own model of medical air compressor, specifically to be used with their flagship Precision Flow device.

Vapotherm 2000i

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Recall controversy

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In 2005, contaminated Vapotherm 2000i respiratory gas humidification devices were associated with an outbreak of Ralstonia mannitolilytica bacteria in children in the United States.[1] Vapotherm issued a recall of all 2000i devices on 13 October 2005.[2] Vapotherm worked with the CDC and FDA to revise the operating manual and reduce risk to patients, and the 2000i was reintroduced on 1 February 2007.[3]

References

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  1. ^ Jhung, M. A.; Sunenshine, R. H.; Noble-Wang, J.; et al. (1 June 2007). "A National Outbreak of Ralstonia mannitolilytica Associated With Use of a Contaminated Oxygen-Delivery Device Among Pediatric Patients". Pediatrics. 119 (6): 1061–1068. doi:10.1542/peds.2006-3739. PMID 17545371. S2CID 23305295. Retrieved 28 July 2015.
  2. ^ "Vapotherm ISSUES URGENT NATIONWIDE RECALL OF All Vapotherm 2000i Respiratory Gas Humidification Devices". Food and Drug Administration. 24 January 2006. Retrieved 28 July 2015.
  3. ^ "FDA Public Health Notification: Precautions in Using the Reintroduced Vapotherm®> 2000i [Respiratory Gas Humidifier] System". Food and Drug Administration. Retrieved 28 July 2015.
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