Monad Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Monad Corp. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Monad Corp. has 9 FDA 510(k) cleared medical devices. Based in Pomona, US.
Historical record: 9 cleared submissions from 1989 to 1991. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Monad Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Monad Corp.
9 devices
Cleared
Dec 17, 1991
MENS 2000-D
Neurology
78d
Cleared
Jun 06, 1991
MY-O-MATIC 5000I
Neurology
385d
Cleared
May 13, 1991
MENS-O-MATIC I
Neurology
248d
Cleared
May 13, 1991
MENS-O-MATIC 2000
Neurology
250d
Cleared
May 13, 1991
MICRO DERM
Neurology
241d
Cleared
May 13, 1991
MENS-O-MATIC 3000
Neurology
241d
Cleared
May 13, 1991
MENS-O-MATIC 1XS AND MENS-O-MATIC 2XS
Neurology
236d
Cleared
May 13, 1991
MENS FREEDOM MICRO
Neurology
250d
Cleared
Apr 25, 1989
PHASER (SINGLE LINEAR MECHANICAL MASSAGE)
Physical Medicine
29d