Philosys, Inc.

FDA Regulatory Profile

Philosys, Inc. has 0 FDA recalls, 2 inspections, 5 510(k) clearances and 1 compliance action on record.

Latest inspection
Mar 30, 2023 · OAI
Latest 510(k)
Dec 1, 2015

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances5Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Mar 30, 2023Gunsan, Korea (The Republic Of)DevicesOfficial Action Indicated (OAI)3010172486
Aug 30, 2018Gunsan, Korea (The Republic Of)DevicesVoluntary Action Indicated (VAI)3010172486

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3010172486Gunsan, Korea (The Republic Of)2Mar 30, 2023

Recent 510(k) Clearances

K-NumberDeviceDate
K151658Gmate Origin Blood Glucose Monitoring SystemDec 1, 2015
K150299Gmate SMART Blood Glucose Monitoring SystemNov 19, 2015
K141656GMATE MINI BLOOD GLUCOSE MONITORING SYSTEM, GMATE STEP BLOOD GLUCOSE MONITORING SYSTEMOct 2, 2015
K131230GMATE SMART BLOOD GLUCOSE MONITORING SYSTEM, GMATE SMART APPLICATIONAug 4, 2014
K113636BLOOD GLUCOSE MONITORING SYSTEM (GLUCOSE OXIDASE)Mar 8, 2013

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