Medical Device Manufacturer · US , New York City , NY

Ever Surplus (Usa), Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

Total

Cleared

Denied

Ever Surplus (Usa), Inc. has 2 FDA 510(k) cleared medical devices. Based in New York City, US.

Historical record: 2 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.

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

Ever Surplus (Usa), 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 - Ever Surplus (Usa), Inc.

2 devices

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