Ito Co., Ltd.

FDA Regulatory Profile

Ito Co., Ltd. has 0 FDA recalls, 7 inspections, 8 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Ito Co., Ltd." and its spelling variants "Ito Co", "Ito".

Latest inspection
Jan 26, 2024 · VAI
Latest 510(k)
May 5, 2021

Reviewing Ito Co., Ltd. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Ito Co., Ltd. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances8Nov 8, 2026File dated Nov 2, 2026Current
Inspections7Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA Record by Year

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

Ito Co., Ltd.: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 1 inspections120242025: 0 inspections020252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202410000
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 FDA Inspections

7 inspections from Apr 20, 2010 to Jan 26, 2024.

DateSiteProductClassificationFEI
Jan 26, 2024Inglewood, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001595422
Oct 10, 2023Hayward, CAFood/CosmeticsNo Action Indicated (NAI)3015144718
May 3, 2019Inglewood, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001595422
Sep 1, 2016Kawaguchi, JapanDevicesVoluntary Action Indicated (VAI)1000533128
May 11, 2016Inglewood, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001595422
Dec 28, 2011Inglewood, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001595422
Apr 20, 2010Inglewood, CAFood/CosmeticsVoluntary Action Indicated (VAI)3001595422

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.

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

3 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3001595422Inglewood, CA5Jan 26, 2024
FEI 3015144718Hayward, CA1Oct 10, 2023
FEI 1000533128Kawaguchi, Japan1Sep 1, 2016

Recent 510(k) Clearances

8 510(k) clearances from Sep 1, 1999 to May 5, 2021.

K-NumberDeviceDate
K203525D functionMay 5, 2021
K112520US-101L, US-103SOct 26, 2011
K081943MODEL ES-130Nov 24, 2008
K081247TM-400Aug 25, 2008
K032793US-100 PORTABLE ULTRASOUND THERAPY UNITOct 9, 2003
K022846SW-180 SHORTWAVE THERAPY UNITJan 28, 2003
K990787TRIO 300Oct 20, 1999
K992545TM-300 TRACTION SYSTEMSep 1, 1999

Need more than this page shows? Ask about Ito Co., Ltd. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

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