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 15, 2026, FDA's public records list Earl-Clay Laboratories with 21 510(k) clearances. The most recent is a 510(k) clearance dated May 13, 1986: ULTRACLONE 01-2300 CELL LINE.
| May 13, 1986 | ULTRACLONE 01-2300 CELL LINEK861585 · KIR | 510(k) clearances |
| May 5, 1986 | ULTRACLONE 01-700 CELL LINEK861569 · KIR | 510(k) clearances |
| Oct 31, 1985 | ULTRACLONE 05-100 GUINEA PIG RBCK854206 · KPO | 510(k) clearances |
| Aug 12, 1985 | ULTRACLONE ECL-01-2200 CELL LINEK853203 · KIR | 510(k) clearances |
| May 10, 1985 | ULTRACLONE ECL-01-800 CELL LINEK851545 · KIR | 510(k) clearances |
| Oct 31, 1984 | ULTRAXLONE ECL-01-1000 CELL LINEK843577 · KIR | 510(k) clearances |
| Oct 31, 1984 | ULTRACLONE ECL-01-1100K843579 · KIR | 510(k) clearances |
| Oct 31, 1984 | ULTRACLONE ECL-01-2100 CELL LINEK843578 · KIR | 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
