Septodont, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Septodont, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Septodont, Inc. has 11 FDA 510(k) cleared dental devices. Based in Walker, US.
Historical record: 11 cleared submissions from 1976 to 1978.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Septodont, Inc.
11 devices
Cleared
Jan 20, 1978
ENDOSOLV E
Dental
22d
Cleared
Jan 04, 1978
NEUTROCIM
Dental
197d
Cleared
Jan 03, 1977
CIMPAT (PINK AND WHITE)
Dental
5d
Cleared
Jan 03, 1977
SELFAST
Dental
5d
Cleared
Nov 24, 1976
FLUOCAL GEL MINT
Dental
47d
Cleared
Nov 24, 1976
FLUOCAL GEL ORANGE
Dental
47d
Cleared
Nov 19, 1976
RACESTYPTINE RINGS
Dental
65d
Cleared
Sep 27, 1976
RACESTYPTINE CORD
Dental
12d
Cleared
Sep 27, 1976
DETARTRINE P
Dental
12d
Cleared
Sep 27, 1976
CALCIPULPE
Dental
12d
Cleared
Sep 27, 1976
HYDROL
Dental
12d