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Euro-Med Intl.

FDA Regulatory Profile

Euro-Med Intl. has 0 FDA recalls, 0 inspections, 16 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Dec 5, 1988

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances16Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K883884PROSTATIC CORE-CUT NEEDLEDec 5, 1988
K882404KEVOR-CURETTEJul 8, 1988
K854891KNIFEMay 2, 1986
K854898ATLANTIC GRASPERMay 2, 1986
K854897MAX-I-GRASPMay 2, 1986
K854896HOOK SCISSORMay 2, 1986
K854894SPOONMay 2, 1986
K854890HOOK PROBEMay 2, 1986
K854895BASKET FORCEPMay 2, 1986
K854901PACIFIC GRASPERMay 2, 1986
K854889FLEX-I-GRASPFeb 21, 1986
K854888RANDALL CURETTEDec 24, 1985
K854893KEYES SKIN PUNCHDec 24, 1985
K854892RULERDec 24, 1985
K854899NOVAK CURETTEDec 24, 1985
K854900EPISIOTOMY SCISSORSDec 24, 1985

FDA data resources