Medical Device Manufacturer · US , Rio Rancho , NM

Lukens Medical Corp. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1991

Recent clearances: LUKENS PGA, (POLYGLYCOLIC ACID) SYNTHETIC ABSORBABLE SURGICAL SUTURE,COATED, BRAIDED-U.S.P.

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.

Lukens Medical Corp. is one of 13008 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Lukens Medical Corp.

8 devices

1-8 of 8

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

General & Plastic Surgery · 118d