Lukens Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lukens Medical Corp. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Lukens Medical Corp. has 8 FDA 510(k) cleared medical devices. Based in Rio Rancho, US.
Historical record: 8 cleared submissions from 1991 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lukens Medical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lukens Medical Corp.
8 devices
Cleared
Feb 12, 1997
LUKENS PGA, (POLYGLYCOLIC ACID) SYNTHETIC ABSORBABLE SURGICAL SUTURE,COATED,...
General & Plastic Surgery
50d
Cleared
Dec 17, 1993
LUKENS STAINLESS STEEL SURGICAL SUTURE
General & Plastic Surgery
297d
Cleared
Dec 17, 1993
LUKENS POLYPROPYLENE MONOFILAMENT NONABSORBABLE
General & Plastic Surgery
297d
Cleared
Dec 17, 1993
LUKENS SILK SURGICAL SUTURE
General & Plastic Surgery
297d
Cleared
Dec 17, 1993
LUKENS NYLON SURGICAL SUTURE
General & Plastic Surgery
297d
Cleared
Dec 17, 1993
LUKENS SURGICAL GUT SUTURE
General & Plastic Surgery
297d
Cleared
Dec 17, 1993
BRAIDED POLYESTER SURGICAL SUTURE
General & Plastic Surgery
297d
Cleared
Jan 30, 1991
LU-TEX II
General & Plastic Surgery
118d