Continuum Electro-Optics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Continuum Electro-Optics, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Continuum Electro-Optics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Santa Clara, US.
Historical record: 7 cleared submissions from 1994 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Continuum Electro-Optics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Continuum Electro-Optics, Inc.
7 devices
Cleared
Feb 20, 2003
MEDLITE Q-SWITHCED LASER
General & Plastic Surgery
190d
Cleared
Oct 16, 2002
DIODENT DENTAL LASER SYSTEM
General & Plastic Surgery
89d
Cleared
Jul 11, 2002
DELIGHT DENTAL ER: YAG LASER SYSTEM
General & Plastic Surgery
56d
Cleared
Feb 27, 2002
DIODENT DENTAL LASER SYSTEM
General & Plastic Surgery
154d
Cleared
Jan 17, 2002
MEDLITE IV Q-SWITCHEDND: YAGLASER REPLACED BY THE MEDLITE C6 Q-SWICTHED ND:...
General & Plastic Surgery
22d
Cleared
Jun 22, 2001
MEDLITE Q-SWITCHED ND:YAG LASER REPLACED BY THE MEDLITE C3 Q-SWTICHED ND:YAG...
General & Plastic Surgery
23d
Cleared
Nov 01, 1994
MULTILITE ERBIUM:YAG SURGICAL LASER SYSTEM
General & Plastic Surgery
497d