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Flux Technology Inc.

FDA Regulatory Profile

Flux Technology Inc. has 1 FDA recall, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Flux Technology Inc." and its spelling variant "Flux Technology".

Latest recall
Z-1878-2025 · Class II · Feb 19, 2025
Latest inspection
Apr 12, 2023 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls1Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Flux Technology Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Flux Technology Inc.: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500010
202400000
202310000
202200000
202100000
202000000
201910000
201800000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent recalls

1 recall record on Feb 19, 2025.

NumberClassProductDate
Z-1878-2025Class IILazervida 10W diode laser cutter and engraver with Lazervida shield.Feb 19, 2025

Recent FDA inspections

2 inspections from Jun 5, 2019 to Apr 12, 2023.

DateSiteProductClassificationFEI
Apr 12, 2023Taipei City, TaiwanDevicesNo Action Indicated (NAI)3015156297
Jun 5, 2019Taipei City, TaiwanDevicesVoluntary Action Indicated (VAI)3015156297
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

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3015156297Taipei City, Taiwan2Apr 12, 2023

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FDA data resources

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