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Reciprocal Labs Corporation

FDA Regulatory Profile

Reciprocal Labs Corporation has 0 FDA recalls, 2 inspections, 10 510(k) clearances and 0 compliance actions on record.

Latest inspection
Aug 2, 2023 · VAI
Latest 510(k)
Mar 26, 2020

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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) clearances10Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 2, 2023San Diego, CADevicesVoluntary Action Indicated (VAI)3009637814
Dec 13, 2018San Diego, CADevicesNo Action Indicated (NAI)3009637814

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
K192724Propeller Sensor for SymbicortMar 26, 2020
K180770Propeller Sensor for NeohalerAug 1, 2018
K161454Propeller Sensor Model 2015-ENov 1, 2016
K152882Propeller SystemMar 8, 2016
K152482Propeller Sensor Model 2014-RMar 4, 2016
K143671Propeller Model 2014-D SensorJun 19, 2015
K142516Propeller SystemMay 15, 2015
K142960Propeller System 2014-RMar 5, 2015
K140638PROPELLER SYSTEM - MODEL 2May 2, 2014
K121609ASTHMAPOLIS SYSTEMJul 2, 2012

FDA data resources