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Protech, Inc.

FDA Regulatory Profile

Protech, Inc. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest 510(k)
Jan 7, 1999

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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) clearances1Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Pro-Tech
Same company group		0700—
Pro-Tech Design And Manufacturing
Same company group		0060—
Pro-Tech Design And Mfg
Same company group		0050—

Recent 510(k) Clearances

K-NumberDeviceDate
K983547PROTECH PLUSJan 7, 1999

FDA data resources

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