Medical Device Manufacturer · US , Mchenry , IL

Beiersdorf, Inc. - FDA 510(k) Cleared Devices

45 submissions · 39 cleared · Since 1977
45
Total
39
Cleared
0
Denied

Beiersdorf, Inc. has 39 FDA 510(k) cleared general & plastic surgery devices. Based in Mchenry, US.

Historical record: 39 cleared submissions from 1977 to 2009.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Beiersdorf, Inc.
45 devices
1-12 of 45

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