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The Sanborn Co.

FDA Regulatory Profile

The Sanborn Co. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "The Sanborn Co." and its spelling variant "Sanborn".

Latest 510(k)
Jul 20, 1990

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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) clearances2Nov 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

2 510(k) clearances from Jun 27, 1990 to Jul 20, 1990.

K-NumberDeviceDate
K901553SURG-K SURGICAL KERATOMETERJul 20, 1990
K901523VKG 1000, VIDEO KERATOGRAPHJun 27, 1990

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FDA data resources

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