Xintec Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Xintec Corporation - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Xintec Corporation has 26 FDA 510(k) cleared general & plastic surgery devices. Based in Oakland, US.
Historical record: 26 cleared submissions from 1990 to 2010.
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 - Xintec Corporation
26 devices
Cleared
Feb 03, 2010
VECTRA PLUS LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
545d
Cleared
Jul 30, 1999
POLARIS DIODE LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
134d
Cleared
Jul 31, 1998
PROTEGE II ER: YAG LASER SYSTEM AND ACCESSOIES (UPGRADE)
General & Plastic Surgery
85d
Cleared
Jul 09, 1998
ALEXIS ALEXANDRITE LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
86d
Cleared
Nov 03, 1997
PROTEGE ER:YAG LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
206d
Cleared
Jun 17, 1997
DENTICA PULSED ND: YAG LASER SYSTEMS AND ACCESSORIES
General & Plastic Surgery
85d
Cleared
Mar 25, 1996
PROTEGE ER:YAG SURGICAL LASER SYSTEM AND ACCESSORIES
General & Plastic Surgery
339d
Cleared
Mar 25, 1996
PRODIGY SUPERPULSE ND:YAG SURGICAL LASER SYSTEMS & ACCESSORIES
General & Plastic Surgery
335d
Cleared
Dec 27, 1995
ODYSSEY HO:YAG SURGICAL LASER SYSTEMS & ACCESSORIES
General & Plastic Surgery
247d
Cleared
Nov 29, 1995
OPTILITE VIII LASER SURGERY ACCESSORIES
General & Plastic Surgery
226d
Cleared
Jan 20, 1995
GENERA 100 SURGICAL SYSTEM
General & Plastic Surgery
88d
Cleared
Jan 06, 1995
OPTILITE (TM) VII FIBEROPTIC ACCESSORIES ROTALASE (TM) ANGLE DELIVERY...
General & Plastic Surgery
105d