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The Belport Company Inc., DBA Gingi-Pak FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

The Belport Company Inc., DBA Gingi-Pak has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "The Belport Company Inc., DBA Gingi-Pak" is on file.

What these totals cover: FDA records filed under the name "The Belport Company Inc., DBA Gingi-Pak" and its spelling variant "Belport Company Inc., Dba Gingi-Pak". Records filed under related names are not included; see Related names.

Latest 510(k): Aug 7, 2026

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	1	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	0	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

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Related names

Each name below has its own page. Its counts cover only the records FDA filed under that name and are not part of the totals for The Belport Company Inc., DBA Gingi-Pak above.

Name	Relation	Recalls	510(k)	Inspections	Compliance actions	Most recent recall
Belport Company Combines 2 spellings Belport Co: 2 510(k)s Belport Company: 4 inspections	Same company group	0	2	4	0	—

Recent 510(k) clearances

1 510(k) clearance on Aug 7, 2026.

K-Number	Device	Date
K261937	PacTemp Automix NE	Aug 7, 2026

The Belport Company Inc., DBA Gingi-Pak and the FDA: common questions

Has The Belport Company Inc., DBA Gingi-Pak received an FDA warning letter?

No FDA warning letter addressed to the name "The Belport Company Inc., DBA Gingi-Pak" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has The Belport Company Inc., DBA Gingi-Pak received an FDA Form 483?

FDA has not published a Form 483 for "The Belport Company Inc., DBA Gingi-Pak" in its reading room. FDA publishes some Form 483s, not all of them.

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