Lukens Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lukens Corp. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Lukens Corp. has 11 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1977 to 1988. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lukens Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lukens Corp.
11 devices
Cleared
Mar 16, 1988
SIXALYZER
Physical Medicine
56d
Cleared
Jan 28, 1980
STANFORD STERILE LAP SPONGES
General & Plastic Surgery
12d
Cleared
Dec 20, 1979
STANFORD STERILE LAP SPONGES
General & Plastic Surgery
17d
Cleared
Sep 24, 1979
LUKENS BONE WAX (GAMMA RADIATION)
General & Plastic Surgery
52d
Cleared
Jul 11, 1977
SHAVE PREP SET
Chemistry
70d
Cleared
Jul 11, 1977
TRAY, CATHETERIZATION W/FOLEY, STERILE
General Hospital
70d
Cleared
Jun 22, 1977
SKIN SCRUB PREP SET
General Hospital
51d
Cleared
Jun 22, 1977
TRAY, IRRIGATION, STERILE, BASIC
General Hospital
51d
Cleared
May 06, 1977
SUTURE REMOVAL SET, STERILE
General & Plastic Surgery
4d
Cleared
May 06, 1977
BLADES, SURGICAL, STERILE
General & Plastic Surgery
4d
Cleared
May 06, 1977
HANDLES, BLADE, SURGICAL
General & Plastic Surgery
4d