Surgidev Corp.

FDA Regulatory Profile

Surgidev Corp. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Surgidev Corp." and its spelling variant "Surgidev".

Latest 510(k)
Apr 9, 1985

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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) clearances4Nov 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

4 510(k) clearances from Jan 26, 1983 to Apr 9, 1985.

K-NumberDeviceDate
K850729ACUFLO VOLUMETRIC CONTROLLED DELIVERY SYS 2000Apr 9, 1985
K831829KARICKHOFF FLYING CORPUSCLE VIEWEROct 19, 1983
K831975LEADING EDGE OPHTHALMIC KNIFEAug 31, 1983
K830008KARICKHOFF KERATOSCOPEJan 26, 1983

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