Combe, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Combe, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Combe, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1994. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Combe, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Combe, Inc.
6 devices
Cleared
Aug 10, 1994
OTC DENTURE CLEANSER
Dental
97d
Cleared
Jan 11, 1993
CFR MONOGRAPH
Dental
84d
Cleared
Sep 19, 1986
SEA-BOND
Dental
16d
Cleared
Oct 10, 1978
FUNGUS FIGHTER INSOLES
General Hospital
162d
Cleared
Jun 24, 1977
CUSHIONS, DENTURE ADHESIVE, ALL-DAY
Dental
112d
Cleared
Feb 04, 1977
SEA-BOND ADHEVISE DENTURE CUSHIONS
General Hospital
9d