Confluent Medical Technologies, Inc.

FDA Regulatory Profile

Confluent Medical Technologies, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Confluent Medical Technologies, Inc." and its spelling variant "Confluent Medical Technologies".

Latest inspection
Aug 15, 2017 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections6Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA inspections

6 inspections from Jun 11, 2009 to Aug 15, 2017.

DateSiteProductClassificationFEI
Aug 15, 2017Fremont, CADevicesNo Action Indicated (NAI)3007635982
Apr 11, 2016Fremont, CADevicesNo Action Indicated (NAI)3007635982
Jan 16, 2014Fremont, CADevicesNo Action Indicated (NAI)3007635982
May 22, 2012Fremont, CADevicesNo Action Indicated (NAI)3007635982
Mar 20, 2012Warwick, RIDevicesVoluntary Action Indicated (VAI)3013668043
Jun 11, 2009Fremont, CADevicesNo Action Indicated (NAI)3007635982
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3007635982Fremont, CA5Aug 15, 2017
FEI 3013668043Warwick, RI1Mar 20, 2012

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.