Device, anti-snoring

FDA product code LRK · Class 2 · 13 devices · 21 reports · 0 devices named in recalls

• Pink Series - H/S SP020US

  Respire Medical Holdings LLC · Device, Anti-Snoring
  3 reports
• Prosomnus IA Monogram

  Prosomnus Sleep Technologies · Device, Anti-Snoring
  3 reports
• ProSomnus EVO Sleep and Snore Device

  Prosomnus Sleep Technologies · Device, Anti-Snoring
  3 reports
• AIRvance® 76353200M

  Medtronic Xomed, Inc. · Device, anti-snoring
  2 reports
• Flex F3000

  Somnomed, Inc. · Device, Anti-Snoring
  2 reports
• Pink Series - EF SP030US

  Respire Medical Holdings LLC · Device, Anti-Snoring
  1 report
• Pink Series - Hard SP000US

  Respire Medical Holdings LLC · Device, Anti-Snoring
  1 report
• Respire Pink+ Hard SPP000US

  Respire Medical Holdings LLC · Device, Anti-Snoring
  1 report
• Respire Pink AT EF SPAT030US

  Respire Medical Holdings LLC · Device, Anti-Snoring
  1 report
• Prosomnus CA Sleep and Snore Device

  Prosomnus Sleep Technologies · Device, Anti-Snoring
  1 report
• ProSomnus EVO Sleep and Snore Device with Patient Monitoring EVO with Patient Monitoring

  Prosomnus Sleep Technologies · Device, Anti-Snoring
  1 report
• The Panthera Anti-Snoring Device 1

  Panthera Dentaire Inc · Device, Anti-Snoring
  1 report
• SICAT OPTISLEEP 10401

  SiCAT GmbH & Co. KG · Device, Anti-Snoring
  1 report