Bien Air USA, Inc. is one of 7747 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bien Air USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ORL-E-92 SURGICAL DRILL SYSTEM, GYRO LONG-LIFE,BLACK PEARL ECO, ONDINE &CROMA, PRESTIGE, BORA, AQUILON, MC2,MC3, BASCH, ISOLITE, OPTIMA, US, PLPE, CA, P
2
Total
2
Cleared
0
Denied
Bien Air USA, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 1998 to 1999. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Bien Air USA, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bien Air USA, Inc.
2 devices