Espe-Premier Sales Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Espe-Premier Sales Co. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Espe-Premier Sales Co. has 10 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1981 to 1981.
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 - Espe-Premier Sales Co.
10 devices
Cleared
Aug 31, 1981
KETAC-CHEM
Dental
35d
Cleared
Aug 31, 1981
PERMAGUM
Dental
35d
Cleared
Aug 31, 1981
PERMAGUM ADHESIVE
Dental
35d
Cleared
Aug 31, 1981
NIMETIC POLISHING PASTE
Dental
35d
Cleared
Aug 31, 1981
NIMETIC-DISPERS
Dental
35d
Cleared
Jun 26, 1981
VISIO-SEAL
Dental
17d
Cleared
Feb 23, 1981
VISIO-BAND
Dental
21d
Cleared
Feb 23, 1981
ETCHING GEL
Dental
21d
Cleared
Jan 14, 1981
ELIPAR LIGHT SOURCE
Dental
27d
Cleared
Jan 14, 1981
VISIO-DISPERS
Dental
26d