Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Lukens Corp. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Mar 16, 1988: SIXALYZER.
| Date | Record | Source |
|---|---|---|
| Mar 16, 1988 | SIXALYZERK880230 · IKK | 510(k) clearances |
| Jan 28, 1980 | STANFORD STERILE LAP SPONGESK800102 · GDY | 510(k) clearances |
| Dec 20, 1979 | STANFORD STERILE LAP SPONGESK792471 · GDY | 510(k) clearances |
| Sep 24, 1979 | LUKENS BONE WAX (GAMMA RADIATION)K791495 · MTJ | 510(k) clearances |
| Jul 11, 1977 | TRAY, CATHETERIZATION W/FOLEY, STERILEK770797 · FRG | 510(k) clearances |
| Jul 11, 1977 | SHAVE PREP SETK770795 · JJX | 510(k) clearances |
| Jun 22, 1977 | SKIN SCRUB PREP SETK770796 · KKX | 510(k) clearances |
| Jun 22, 1977 | TRAY, IRRIGATION, STERILE, BASICK770799 · KKX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
