Medical Device Manufacturer · US , South San Francisco , CA

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

2 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

Bionike, Inc. has 2 FDA 510(k) cleared medical devices. Based in South San Francisco, US.

Historical record: 2 cleared submissions from 1997 to 1999. Primary specialty: Toxicology.

Browse the FDA 510(k) cleared devices submitted by Bionike, Inc. Filter by specialty or product code using the sidebar.

Bionike, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Bionike, Inc.

2 devices

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