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510k Database
Manufacturers
US
Dfine, Inc.
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Medical Device Manufacturer
·
US , Cupertino , CA
Dfine, Inc. - FDA 510(k) Cleared Devices
5 submissions
·
5 cleared
·
Since 2006
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dfine, Inc.
General & Plastic Surgery
✕
1
devices
1-1 of 1
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Cleared
Aug 11, 2010
ABLATION INSTRUMENT, MODEL 1635
K091310
·
GEI
General & Plastic Surgery
·
464d
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5
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4
General & Plastic Surgery
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