Rolence Ent., Inc. is one of 203 FDA 510(k) medical device manufacturers from Taiwan in the dataset, ranked by real submission volume.
Rolence Ent., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Rolence Ent., Inc. has 5 FDA 510(k) cleared medical devices. Based in Chungli, TW.
Historical record: 5 cleared submissions from 2002 to 2009. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Rolence Ent., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rolence Ent., Inc.
5 devices
Cleared
Dec 16, 2009
ROLENCE DENTAL HIGH SPEED HANDPIECE, RHP
Dental
76d
Cleared
Dec 30, 2002
ULTRA-LITE 200E LIGHT CURE UNIT
Dental
69d
Cleared
Jun 12, 2002
ULTRA-LITE 5 TURBO LIGHT CURE UNIT
Dental
86d
Cleared
Jun 12, 2002
EXCELLITE TURBO LIGHT CURE UNIT
Dental
86d
Cleared
Jun 12, 2002
EXCELLITE LIGHT CURE UNIT
Dental
86d