Midwest Orthodontic Mfg. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Midwest Orthodontic Mfg. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Midwest Orthodontic Mfg. has 7 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 7 cleared submissions from 1990 to 1998. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Midwest Orthodontic Mfg. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Midwest Orthodontic Mfg.
7 devices
Cleared
Jun 25, 1998
ORTHODONTIC BRACES
Dental
66d
Cleared
Feb 08, 1996
GLUFLORMA
Dental
55d
Cleared
Sep 12, 1995
LIGHT-CURE PC
Dental
82d
Cleared
Sep 08, 1995
PC-LOCK
Dental
78d
Cleared
Sep 05, 1995
PRO-LOCK
Dental
75d
Cleared
Sep 05, 1995
LIGHT-CURE
Dental
75d
Cleared
May 22, 1990
FLUOR-I-CHAINS(TM) AND FLUOR-I-TIES(TM)
Dental
90d