Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Huntington Laboratories, Inc. with 7 510(k) clearances and 2 drug applications. The most recent is a 510(k) clearance dated Mar 12, 1996: ASCEND GENERAL PURPOSE DISINFECTANT.
| Mar 12, 1996 | ASCEND GENERAL PURPOSE DISINFECTANTK960582 · LRJ | 510(k) clearances |
| Mar 12, 1996 | MATAR GENERAL PURPOSE DISINFECTANTK960583 · LRJ | 510(k) clearances |
| Mar 12, 1996 | BEAUCOUP GENERAL PURPOSE DISINFECTANTK960580 · LRJ | 510(k) clearances |
| Aug 11, 1995 | FORMULATION HWS-128 EPA REG. NO. 47371-130K953009 · LRJ | 510(k) clearances |
| Aug 11, 1995 | FORMULATION HWS-64 EPA REG. NO. 47371-131K953011 · LRJ | 510(k) clearances |
| Aug 11, 1995 | FORMULATION HWS-256 EPA REG. NO. 47371-129K953010 · LRJ | 510(k) clearances |
| Nov 13, 1985 | SANA-LUBEK853653 · KMJ | 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
