Medical Device Manufacturer · US , Burlingame , CA

Bell Intl., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

Bell Intl., Inc. has 2 FDA 510(k) cleared medical devices. Based in Burlingame, US.

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

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

Bell Intl., 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 - Bell Intl., Inc.

2 devices

1-2 of 2