Hoya Conbio, Inc. is one of 21644 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hoya Conbio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: REVLITE Q-SWITCHED ND:YAG LASER SYSTEM, SCULPTURE 2.94 ER:YAG SYSTEM, V-RASER DIODE LASER SYSTEM
7
Total
7
Cleared
0
Denied
Hoya Conbio, Inc. has 7 FDA 510(k) cleared medical devices. Based in Fremont, US.
Historical record: 7 cleared submissions from 2006 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hoya Conbio, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hoya Conbio, Inc.
7 devices
Cleared
Jun 01, 2009
REVLITE Q-SWITCHED ND:YAG LASER SYSTEM
General & Plastic Surgery
154d
Cleared
Aug 27, 2008
SCULPTURE 2.94 ER:YAG SYSTEM
General & Plastic Surgery
293d
Cleared
Feb 14, 2008
V-RASER DIODE LASER SYSTEM
General & Plastic Surgery
79d
Cleared
Mar 16, 2007
DIODENT MICRO DENTAL LASER SYSTEM, MODELS 810 AND 980
General & Plastic Surgery
128d
Cleared
Jan 25, 2007
REVLITE C6 Q-SWITCHED ND:YAG LASER SYSTEM
General & Plastic Surgery
30d
Cleared
Dec 01, 2006
REVLITE Q-SWITCHED ND:YAG LASER
General & Plastic Surgery
51d
Cleared
May 24, 2006
MEDLITE C SERIES COMPRESSION TOOL AND HANDPIECE ATTACHMENT ACCESSORY, MODEL...
General & Plastic Surgery
44d