Medical Device Manufacturer · US , Burlington , VT

A and V Ent. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1993

Total

Cleared

Denied

A and V Ent. has 1 FDA 510(k) cleared medical devices. Based in Burlington, US.

Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by A and V Ent. Filter by specialty or product code using the sidebar.

A and V Ent. 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 - A and V Ent.

1 devices

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