Astron Dental Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Astron Dental Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Astron Dental Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1983 to 1987. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Astron Dental Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Astron Dental Corp.
5 devices
Cleared
Dec 23, 1987
2ND MODIFIED VINYLAC PRESS PACK DENTURE RESIN
Dental
82d
Cleared
Feb 10, 1987
MODIFIED VINYLAC PRESS PACK DENTURE RESIN
Dental
67d
Cleared
Jul 31, 1985
DURACLEAN DENTURE CLEANER
Dental
22d
Cleared
Jul 19, 1984
ASTRON 77 INJECTION DENTURE RESIN
Dental
302d
Cleared
Jun 08, 1983
VINYLAC PRESS-PACK DENTURE RESIN
Dental
51d