Medical Device Manufacturer · US , Westport , CT

Fiber Mesh, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

Fiber Mesh, Inc. has 1 FDA 510(k) cleared medical devices. Based in Westport, US.

Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Dental.

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

Fiber Mesh, 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 - Fiber Mesh, Inc.

1 devices

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