Rolence Enterprise Co. , Ltd.
Rolence Enterprise Co. , Ltd. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2000.
Top product codes for Rolence Enterprise Co. , Ltd.
Recent clearances by Rolence Enterprise Co. , Ltd.
- K001719 — Q-LUX PLASMA 100 LIGHT CURE UNIT
- K991865 — Q-LITE 75 LIGHT CURE UNIT
- K991863 — CUTE-LITE I LIGHT CURE UNIT
- K980792 — CU-100A LIGHT CURE UNIT
- K980793 — Q-LUXPRO V/Q-LUXPRO II LIGHT CURE UNIT
- K960351 — Q-LUX LIGHT CURE UNIT
- K960364 — CU-200 LIGHT CURE UNIT
- K953628 — PROPHY ANGLE
- K952423 — CU-100RLC LIGHT CURE UNIT, DOCUMENT NO.A715676
- K942199 — CU-100R LIGHT CURE UNIT, DOCUMENT NO. A715676
- K942198 — CU-80 LIGHT CURE UNIT, DOCUMENT NO. A715676
- K924727 — 100 LIGHT CURE UNIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.