Aladan Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aladan Corp. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Aladan Corp. has 18 FDA 510(k) cleared general hospital devices. Based in Jessup, US.
Historical record: 18 cleared submissions from 1989 to 1996.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aladan Corp.
18 devices
Cleared
Oct 31, 1996
TRI-CLEAN 110/TRI-CLEAN PLUS GLOVE
General Hospital
262d
Cleared
Jul 20, 1995
SAFETEX SUPER HYPERALLERGENIC POWDERFREE LATEX MEDICAL GLOVE
General Hospital
59d
Cleared
Jun 26, 1995
SAFETEX SUPER HYPOALLERGENIC POWDERED LATEX EXAMINATION GLOVE
General Hospital
24d
Cleared
Jun 22, 1995
SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM
Obstetrics & Gynecology
314d
Cleared
Jun 15, 1995
ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES
General Hospital
56d
Cleared
Apr 14, 1995
SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM
Obstetrics & Gynecology
248d
Cleared
Jul 08, 1994
HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE
General Hospital
25d
Cleared
Apr 22, 1994
SAFETEX HYPOALLERGENIC POWDERFREE LATEX EXAMINATION GLOVE
General Hospital
56d
Cleared
May 03, 1991
ALADAN LATEX MEDICAL GLOVE
General Hospital
14d
Cleared
Apr 16, 1991
LATEX EXAMINATION GLOVES (HYPOALLERGENIC)
General Hospital
39d
Cleared
Feb 19, 1991
CONDOM (RUBBER) CONTRACEPTIVE
Obstetrics & Gynecology
88d
Cleared
Jan 18, 1991
ALADERM
General Hospital
30d