St. George Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
St. George Technology, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
St. George Technology, Inc. has 4 FDA 510(k) cleared medical devices. Based in York, US.
Historical record: 4 cleared submissions from 1994 to 2003. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by St. George Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - St. George Technology, Inc.
4 devices
Cleared
Feb 14, 2003
ST. GEORGE TECHNOLOGY, INC PERFECTION PLUS DISPOSABLE PROPHY ANGLE
Dental
79d
Cleared
Feb 10, 2000
EXCEL ULTRA-HI FORMULA HEAT-CURED DENTURE BASE MATERIAL
Dental
227d
Cleared
Feb 02, 1995
EXCEL-P FORMULA AUTO-CURE DENTURE BASE
Dental
73d
Cleared
Jan 18, 1994
EXCEL FORMULA HEAT-AUTO CURE DENT BASE/REPAIR/ORTHO
Dental
154d