Shanghai Glovmax Enterprise Co.,Ltd

FDA Regulatory Profile

Shanghai Glovmax Enterprise Co.,Ltd 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 "Shanghai Glovmax Enterprise Co.,Ltd" and its spelling variant "Shanghai Glovmax Enterprise Co".

Latest 510(k)
May 31, 2002

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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 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) clearances

4 510(k) clearances from Jan 12, 2000 to May 31, 2002.

K-NumberDeviceDate
K021000SHANGHAI GLOVMAX ENTERPRISE POWDERED BLUE NITRILE EXAMINATION GLOVESMay 31, 2002
K021001SHANGHAI GLOVMAX ENTERPRISE POWDERFREE BLUE NITRILE EXAMINATION GLOVESMay 16, 2002
K993880SHANGHAI GLOVMAX ENTERPRISE CO, LTD., POWDER-FREE VINYL PATIENT EXAMINATION GLOVESJan 12, 2000
K993859SHANGHAI GLOVMAX ENTERPRISE CO., LTD. PRE-POWDERED VINYL PATIENT EXAMINATION GLOVESJan 12, 2000

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