Sunrise Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sunrise Technologies, Inc. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
0
Denied
Sunrise Technologies, Inc. has 17 FDA 510(k) cleared general & plastic surgery devices. Based in Mountain View, US.
Historical record: 17 cleared submissions from 1990 to 1996.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sunrise Technologies, Inc.
18 devices
Cleared
Sep 03, 1996
SUNRISE CURING LAMP
Dental
88d
Cleared
Sep 01, 1994
SLASE 210 PLUS HOLMIUM LASER SYSTEM
General & Plastic Surgery
97d
Cleared
Apr 25, 1994
MICROPREP CAVITY PREPERATION SYSTEM
Dental
311d
Cleared
Jan 10, 1994
SLASE 210 & SLASE 210 PLUS HOLMIUM LASER SYSTEMS
General & Plastic Surgery
203d
Cleared
Jul 26, 1993
MODEL 5030 SUCTION HANDPIECE SYSTEM
General & Plastic Surgery
35d
Cleared
Jul 22, 1993
UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER
General & Plastic Surgery
104d
Cleared
May 21, 1993
8-WATT PULSED DENTAL LASER SYSTEM
General & Plastic Surgery
94d
Cleared
May 21, 1993
2.5 WATT PULSED DENTAL LASER SYSTEM
General & Plastic Surgery
91d
Cleared
Mar 09, 1993
SLASE 210 PLUS HOLMIUM LASER SYSTEM
General & Plastic Surgery
126d
Cleared
Jul 21, 1992
MODEL SLASE 210 HOLMIUM LASER SYSTEM
General Hospital
182d
Cleared
Mar 13, 1992
ADL 400 ND
General & Plastic Surgery
64d
Cleared
Mar 13, 1992
ADL 800 ND:YAG LASER SYSTEM FOR INTRAORAL TIS. SUR
General & Plastic Surgery
64d