Espe Dental Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Espe Dental Products - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Espe Dental Products has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1977 to 1981. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Espe Dental Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Espe Dental Products
8 devices
Cleared
Apr 29, 1981
VISIO-SEAL
Dental
22d
Cleared
Nov 24, 1980
KETAC-CEM IN REF. TO K802048
Dental
17d
Cleared
Sep 16, 1980
NIMETIC-DISPERS
Dental
22d
Cleared
Feb 05, 1980
PERMADYNE POLYETHER RUBBER IMPRESSION
Dental
29d
Cleared
Oct 20, 1977
UNIOLITE
Dental
14d
Cleared
Oct 20, 1977
CAPMIX
Dental
13d
Cleared
Aug 03, 1977
IMPREFLEX ALGINATE IMPRESSION MATERIAL
Toxicology
42d
Cleared
Jul 15, 1977
PASTES, RESTORATIVE & TINTED, DEBTAL
Dental
23d