Midwest is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Midwest - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Midwest has 13 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1976 to 1986.
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 - Midwest
13 devices
Cleared
Oct 06, 1986
TRADITION HIGH SPEED HANDPIECE
Dental
17d
Cleared
Mar 25, 1985
AM-40 POWER OPTIC AIR MOTOR POWER OPTIC CONTRA ANG
Dental
56d
Cleared
Dec 06, 1979
MW STRAIGHT ATTACHMENT
Dental
6d
Cleared
Nov 27, 1979
LS-100
Dental
11d
Cleared
Nov 27, 1979
MW 8000-I
Dental
11d
Cleared
Nov 27, 1979
MW-8000
Dental
11d
Cleared
Nov 20, 1979
ORALUMINATOR III AUTO-LIGHT
Dental
74d
Cleared
Oct 23, 1979
LIGHT-PAK
Dental
56d
Cleared
Feb 26, 1979
MIDWEST 1000
Dental
38d
Cleared
Dec 29, 1978
LIGHT, INSIDE
Dental
53d
Cleared
Oct 20, 1976
FIBER OPTICS HIGH SPEED HANDPIECE
Dental
12d
Cleared
Oct 20, 1976
FIBER OPTICS DENTAL HOSE W/INTEGRAL L.C.
Dental
12d