Medi-Spec

FDA Regulatory Profile

Medi-Spec has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Medi-Spec". Records filed under related names are not included; see Related names.

Latest 510(k)
Feb 4, 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) clearances8Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) clearances

8 510(k) clearances from Aug 21, 1978 to Feb 4, 1984.

K-NumberDeviceDate
K833068LAMINARIA JAPONICA CERVICAL DILATORFeb 4, 1984
K812694WHISK-ROct 26, 1981
K812426UTERINE ASPIRATION CURETTES(RIGID&FLEX)Oct 8, 1981
K801554STERILE CAST PADDINGAug 4, 1980
K800404MEDSPEC OPERATIVE OPTHALMIC KITApr 24, 1980
K800490STERILE DRESSING PACKMar 12, 1980
K790952CLAMP COVERSJun 5, 1979
K780548DISPOSA-LOOPSAug 21, 1978

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