Davis Schottlander & Davis, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Davis Schottlander & Davis, Ltd. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Davis Schottlander & Davis, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Kansas City, US.
Historical record: 7 cleared submissions from 1996 to 2004. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Davis Schottlander & Davis, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Davis Schottlander & Davis, Ltd.
7 devices
Cleared
Jan 22, 2004
MATCH MASTER LOW FUSION PORCELAIN
Dental
395d
Cleared
Aug 25, 2003
MATCH PRESS PRESSABLE CERAMIC
Dental
245d
Cleared
Jun 16, 2000
SCHOTTLANDER ENIGMA COLOUR TONE, MODEL 0156
Dental
37d
Cleared
Dec 22, 1999
ENIGMA HI-BASE DENTURE BASE MATERIAL
Dental
49d
Cleared
Feb 12, 1999
NATURA DENTURE TEETH
Dental
86d
Cleared
Feb 09, 1999
ENIGMA DENTURE TEETH
Dental
83d
Cleared
Nov 19, 1996
MATCHMAKER/PROPAQUE PORCELAIN
Dental
267d