Bien Air USA, Inc.

Bien Air USA, Inc. holds 2 FDA 510(k) medical device clearances, first cleared 1998, most recent 1999.

Top product codes for Bien Air USA, Inc.

EFB — Dental2 devices

Recent clearances by Bien Air USA, Inc.

K984244 — ORL-E-92 SURGICAL DRILL SYSTEMCode EFB·1999-02-23
K983183 — GYRO LONG-LIFE,BLACK PEARL ECO, ONDINE &CROMA, PRESTIGE, BORA, AQUILON, MC2,MC3, BASCH, ISOLITE, OPTIMA, US, PLPE, CA, PCode EFB·1998-12-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.