Airway Management, Inc.

FDA Regulatory Profile

Airway Management, Inc. has 0 FDA recalls, 4 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest inspection
Oct 5, 2022 · NAI
Latest 510(k)
Sep 11, 2025

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances7Oct 4, 2026Not statedCurrent
Inspections4Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Oct 5, 2022Farmers Branch, TXDevicesNo Action Indicated (NAI)3003496134
Mar 13, 2020Farmers Branch, TXDevicesVoluntary Action Indicated (VAI)3003496134
Jun 14, 2017Farmers Branch, TXDevicesVoluntary Action Indicated (VAI)3003496134
Jun 21, 2013Farmers Branch, TXDevicesNo Action Indicated (NAI)3003496134

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K252374Nylon flexTAP(R)Sep 11, 2025
K181482myTAP2Aug 31, 2018
K160239TAP 3, TAP 1Aug 10, 2016
K122350TAP PAP NASAL PILLOW MASKNov 1, 2012
K062951TAP III ANTI-SNORING DEVICEDec 12, 2006
K061732TAP-TJul 12, 2006
K060388TAP II ANTI-SNORING AND OBSTRUCTIVE SLEEP APNEA ORAL APPLIANCE WITH ATTACHMENTMay 17, 2006