Flexitech Sdn. Bhd. is one of 78 FDA 510(k) medical device manufacturers from Malaysia in the dataset, ranked by real submission volume.
Flexitech Sdn. Bhd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Flexitech Sdn. Bhd. has 6 FDA 510(k) cleared medical devices. Based in Klang, Selangor, MY.
Historical record: 6 cleared submissions from 1999 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Flexitech Sdn. Bhd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Flexitech Sdn. Bhd.
6 devices
Cleared
Feb 03, 2000
POLYMER COATED POWDER FREE NITRILE EXAMINATION GLOVES, BLUE
General Hospital
36d
Cleared
Jan 31, 2000
POLYMER COATED, POWDER FREE, LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT...
General Hospital
39d
Cleared
Apr 02, 1999
POWDER FREE NITRILE EXAMINATION GLOVES
General Hospital
44d
Cleared
Apr 02, 1999
PREPOWDERED NITRILE EXAMINATION GLOVES
General Hospital
44d
Cleared
Apr 02, 1999
POWDER FREE LATEX EXAMINATION GLOVES, W/ PROTEIN LABELING CLAIM
General Hospital
44d
Cleared
Apr 02, 1999
PREPOWDERED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (100...
General Hospital
44d