Guangzhou Ekai Electronic Technology Co., Ltd. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • No warning letters matched by name
Inspections 0 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 1 Latest Aug 11, 2023

Guangzhou Ekai Electronic Technology Co., Ltd. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Guangzhou Ekai Electronic Technology Co., Ltd." is on file.

What these totals cover: FDA records filed under the name "Guangzhou Ekai Electronic Technology Co., Ltd." and its spelling variant "Guangzhou Ekai Electronic Technology Co".

Latest 510(k)
Aug 11, 2023

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances1Nov 15, 2026File dated Nov 9, 2026Current
Inspections0Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent 510(k) clearances

1 510(k) clearance on Aug 11, 2023.

K-NumberDeviceDate
K230420Dr. pen Microneedling SystemAug 11, 2023

Guangzhou Ekai Electronic Technology Co., Ltd. and the FDA: common questions

Has Guangzhou Ekai Electronic Technology Co., Ltd. received an FDA warning letter?

No FDA warning letter addressed to the name "Guangzhou Ekai Electronic Technology Co., Ltd." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Guangzhou Ekai Electronic Technology Co., Ltd. received an FDA Form 483?

FDA has not published a Form 483 for "Guangzhou Ekai Electronic Technology Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.

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