Scanlan Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Scanlan Intl., Inc. - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Scanlan Intl., Inc. has 19 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1978 to 1996. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Scanlan Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Scanlan Intl., Inc.
19 devices
Cleared
Apr 26, 1996
SCANLAN HEIFETZ ANEURYSM ELGILOY CLIP SYSTEM
Neurology
91d
Cleared
Dec 05, 1994
SCANLAN(R) THORACOSCOPIC SCISSORS, CLAMP, FORCEPS, NEEDLE HOLDER
General & Plastic Surgery
27d
Cleared
Feb 18, 1992
SCANLAN/TAHERI VALVULOTOME
Cardiovascular
337d
Cleared
Jan 12, 1987
SCANLAN (TM) VEIN/GRAFT HOLDER
Cardiovascular
27d
Cleared
Jan 12, 1987
SCANLAN (TM) INSTRUMENT TRAY
General & Plastic Surgery
27d
Cleared
Jul 12, 1985
SCANLAN TUNNELER, SHEATH & TIP
Cardiovascular
77d
Cleared
Aug 03, 1984
SCANLAN ENDARSECTOR
Cardiovascular
113d
Cleared
Jul 06, 1984
SCANLAN ATRAUM INSTRUMENT JAW COVER
General & Plastic Surgery
85d
Cleared
Jun 11, 1984
SCANLAN COLORMARK SKIN MARKER
General & Plastic Surgery
90d
Cleared
Jun 05, 1984
SCANLAN VASCU-STATT II APPROXIMATOR
General & Plastic Surgery
54d
Cleared
Jun 05, 1984
SCANLAN VASCU-STATT II
Ophthalmic
54d
Cleared
Apr 24, 1984
SURGICAL INSTRUMENT DEMAGNETIZER
General & Plastic Surgery
42d
Cleared
Mar 24, 1983
SCANLAN SINGLE-USE AORTA PUNCH
Cardiovascular
100d
Cleared
Jan 07, 1983
VASCU-STATT APPROXIMATOR
General & Plastic Surgery
30d
Cleared
Jul 28, 1982
SCANLAN SUTURE-STATT
General & Plastic Surgery
33d
Cleared
Mar 13, 1981
SCANLAN SUTURE BOOTS
Hematology
18d
Cleared
Jan 15, 1981
SCANLAN VASCU-STATT
General Hospital
66d
Cleared
Sep 26, 1980
SCANLAN STERNUM NEEDLE-SUTURE
General & Plastic Surgery
38d
Cleared
Apr 18, 1978
NEEDLE DRIVER
General & Plastic Surgery
61d