# Lukens Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 11 (1977–1988): 11 510(k) clearances
- Product codes: GES (2), KKX (2), GDY (2), FRG (1), JJX (1), KDC (1), IKK (1), MTJ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Orthocon, Inc.: 1 (https://510kreport.com/company/orthocon)
- Skeletal Kinetics, LLC: 1 (https://510kreport.com/company/skeletal-kinetics)
- Ceremed, Inc.: 1 (https://510kreport.com/company/ceremed)
- United States Surgical, A Division of Tyco Healthc: 1 (https://510kreport.com/company/united-states-surgical-a-division-of-tyco-healthc)
- Cp Medical: 1 (https://510kreport.com/company/cp-medical)

## Its most-cited devices
- K791495: Lukens Bone Wax (Gamma Radiation) (1979), cited by 5

## Recent decisions
- K880230: Sixalyzer (Mar 16, 1988)
- K800102: Stanford Sterile Lap Sponges (Jan 28, 1980)
- K792471: Stanford Sterile Lap Sponges (Dec 20, 1979)
- K791495: Lukens Bone Wax (Gamma Radiation) (Sep 24, 1979)
- K770797: Tray, Catheterization W/Foley, Sterile (Jul 11, 1977)
- K770795: Shave Prep Set (Jul 11, 1977)
- K770799: Tray, Irrigation, Sterile, Basic (Jun 22, 1977)
- K770796: Skin Scrub Prep Set (Jun 22, 1977)

Source page: https://510kreport.com/company/lukens