Spiration, Inc.

FDA Regulatory Profile

Spiration, Inc. has 0 FDA recalls, 0 inspections, 5 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Nov 20, 2017

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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) clearances5Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K171492B7 2C Occlusion BalloonNov 20, 2017
K170990Active Needle Endoscopic Treatment (ANET) Electrosurgical ApplicatorMay 11, 2017
K162611PeriFLEXFeb 9, 2017
K152922ViziShot FLEXFeb 19, 2016
K142909Flexible 19G EBUS NeedleApr 24, 2015