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Unomedical Devices S.A DE C.V.

FDA Regulatory Profile

Unomedical Devices S.A DE C.V. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Unomedical Devices S.A DE C.V." and its spelling variant "Unomedical Devices S.A De C.V".

Latest 510(k)
May 30, 2012

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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 May 30, 2012.

K-NumberDeviceDate
K120395NERIA MULTI SUBCUTANEOUS INFUSION SETMay 30, 2012

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FDA data resources

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