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Hans Biomed Corp.

FDA Regulatory Profile

Hans Biomed Corp. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 21, 2016.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K152077MaxiGenApril 21, 2016
K151271BellaFuseMarch 11, 2016
K130235SURFUSE II GEL, SURFUSE II PUTTY, EXFUSE II GEL, EXFUSE II PUTTYJanuary 10, 2014
K113728SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTYNovember 15, 2012

FDA data resources