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510(k) K052862

FULL BREATH SLEEP APPLIANCE - AB (ANTERIOR BITE) by Bryan Keropian Dds — Product Code LQZ

K052862 is an FDA 510(k) premarket notification submitted by Bryan Keropian Dds for the device "FULL BREATH SLEEP APPLIANCE - AB (ANTERIOR BITE)". The FDA issued a decision of Substantially Equivalent on December 30, 2005. The device falls under product code LQZ (Device, Jaw Repositioning), a Class II device regulated under 21 CFR 872.5570. Bryan Keropian Dds has at least 3 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 30, 2005
Date Received
October 11, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Jaw Repositioning
Device Class
Class II
Regulation Number
872.5570
Review Panel
DE
Submission Type

Other clearances by Bryan Keropian Dds

  • K091035 — FULL BREATH SLEEP APPLIANCE LOWER (FBSL) (June 24, 2009)
  • K061228 — FULL BREATH SLEEP APPLIANCE WITH POSTERIOR TONGUE DEPRESSOR (May 26, 2006)
  • K053065 — FULL BREATH SLEEP APPLIANCE - PB (POSTERIOR BITE AND PBB (POSTERIOR BITE WITH BU (January 3, 2006)

Other clearances for product code LQZ

  • K233754 — AIO Breathe (February 23, 2024)
  • K230532 — RADx Intraoral Appliance for Snoring and Sleep Apnea (July 12, 2023)
  • K203712 — The Slide (July 20, 2021)
  • K191320 — Slow Wave DS8 (October 2, 2020)
  • K192581 — The NightBlocks Appliance (January 28, 2020)
  • K162816 — SML-OSA2 Appliances (July 27, 2017)
  • K130130 — ATG/SM-OSA APPLIANCES (August 26, 2013)
  • K112627 — MILLENIUM ANTI-SNORING DEVICE (June 6, 2012)
  • K112766 — SNORKEL (June 4, 2012)
  • K113201 — NARVAL CC (December 1, 2011)

FDA data resources