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 its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list American Bantex with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 21, 2004: AMERICAN BANTEX, MODEL MS 3.
| Oct 21, 2004 | AMERICAN BANTEX, MODEL MS 3K042104 · INI | 510(k) clearances |
| Oct 20, 2004 | AMERICAN BANTEX HUMIDIFIER, DRY, BUBBLE, MODELS B9000, 3 PSI AND B9100, 6 PSIK041963 · BTT | 510(k) clearances |
| Jul 23, 2004 | AMERICAN BANTEX MS 4 MINI SCOOTERK040754 · INI | 510(k) clearances |
| Dec 18, 2003 | TANGO, MODELS, BP1K031711 · ITI | 510(k) clearances |
| Oct 30, 1996 | BANTEX SURGICAL LATEX GLOVES- TYPE 1 NATURAL RUBBER LATEX SURGICSL GLOVES, STERILEK963218 · KGO | 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
