FDA 510(k) Applications Submitted by STERLING CHENG

FDA 510(k) Number Submission Date Device Name Applicant
K960351 01/25/1996 Q-LUX LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K960364 01/25/1996 CU-200 LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K040396 02/17/2004 ULTRASONIC SCALER ELEGANCE MS-10 (25K) ROLENCE ENTEPRISE, INC.
K980792 03/02/1998 CU-100A LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K980793 03/02/1998 Q-LUXPRO V/Q-LUXPRO II LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K020874 03/18/2002 ULTRA-LITE 5 TURBO LIGHT CURE UNIT ROLENCE ENT. INC.
K020877 03/18/2002 EXCELLITE TURBO LIGHT CURE UNIT ROLENCE ENT. INC.
K020884 03/18/2002 EXCELLITE LIGHT CURE UNIT ROLENCE ENT. INC.
K991863 06/01/1999 CUTE-LITE I LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K991865 06/01/1999 Q-LITE 75 LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K001719 06/05/2000 Q-LUX PLASMA 100 LIGHT CURE UNIT ROLENCE ENTERPRISE CO. LTD.
K172928 09/25/2017 Portable X-ray System Rolence Enterprise Inc.
K023545 10/22/2002 ULTRA-LITE 200E LIGHT CURE UNIT ROLENCE ENT. INC.
K043325 12/02/2004 ZOOMCAM LD-10 INTRAORAL CAMERA AND ACCESSORIES ROLENCE ENTEPRISE, INC.


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