Diverse Technologies, Inc. FDA Record

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

Diverse Technologies, Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Diverse Technologies, Inc." is on file.

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

Latest 510(k)
Jan 27, 1984

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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) clearances1Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) clearances

1 510(k) clearance on Jan 27, 1984.

K-NumberDeviceDate
K833467SURE-CUTJan 27, 1984

Diverse Technologies, Inc. and the FDA: common questions

Has Diverse Technologies, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Diverse Technologies, Inc." 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 Diverse Technologies, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Diverse Technologies, Inc." 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.