Gallini Intl., Inc.

FDA Regulatory Profile

Gallini Intl., Inc. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Gallini Intl., Inc." and its spelling variant "Gallini Intl".

Latest 510(k)
May 21, 1997

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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) clearances7Nov 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

7 510(k) clearances from Nov 21, 1996 to May 21, 1997.

K-NumberDeviceDate
K970872PAN (CHIBA ASPIRATING NEEDLE)May 21, 1997
K970871TR NEEDLEMay 21, 1997
K964777TZJan 3, 1997
K962570ISAN STERNAL-ILIAC ASPIRATION BIOPSY NEEDLENov 27, 1996
K962569BIOMID BONE MARROW BIOPSY NEEDLENov 27, 1996
K962568ACRI ILIAC CREST ASPIRATION BIOPSY NEEDLESNov 25, 1996
K961407SPEED-CUTNov 21, 1996

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