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 14, 2026, FDA's public records list Kenlor Industries with 9 510(k) clearances. The most recent is a 510(k) clearance dated Mar 3, 1997: KENLOR H. PYLORI CONTROL SERUM.
| Mar 3, 1997 | KENLOR H. PYLORI CONTROL SERUMK964014 · LYR | 510(k) clearances |
| Jul 19, 1995 | KENLOR LIQUID TOTAL URINE CONTROLK952840 · JJW | 510(k) clearances |
| Mar 20, 1995 | KENLOR HUMAN SPINAL FLUID CONTROLK950326 · JJY | 510(k) clearances |
| Sep 7, 1990 | KENLOR THERAPEUTIC DRUG MONITORING (TDM) CONTROLK903338 · JJY | 510(k) clearances |
| Feb 16, 1990 | KENLOR PYROGALLOL RED MICROPROTEIN ASSAY KITK896440 · JIR | 510(k) clearances |
| May 22, 1989 | COOMASSIE BLUE TOTAL PROTEIN ASSAY KITK890618 · CEK | 510(k) clearances |
| Mar 24, 1989 | KENLOR TOTAL IRON, UIBC/TIBC ASSAY KITK890573 · JIY | 510(k) clearances |
| Mar 9, 1989 | KENLOR LIQUID URINE CONTROLK890577 · JJW | 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
