Unicare Medical Products, Inc. FDA Record

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

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

What these totals cover: FDA records filed under the name "Unicare Medical Products, Inc." and its spelling variant "Unicare Medical Products".

Latest 510(k)
Jul 15, 1986

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

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Recent 510(k) clearances

1 510(k) clearance on Jul 15, 1986.

K-NumberDeviceDate
K861608UNICARE BREAST SHELLSJul 15, 1986

Unicare Medical Products, Inc. and the FDA: common questions

Has Unicare Medical Products, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Unicare Medical Products, 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 Unicare Medical Products, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Unicare Medical Products, 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.