Medical device makerLabelled 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 13, 2026, FDA's public records list Maytex Corp with 4 510(k) clearances and 1 device recall. The most recent is a device recall dated May 15, 2013: Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G….
| Date | Record | Source |
|---|---|---|
| May 15, 2013 | Comfort brand Ear-Loop Face Mask, Item #: 3100, Model Numbers: # 3100B, # 3100P, # 3100G, # 3100Y, # 3100W; Product is manufactured and distClass II · Recent Lab testing conducted in March 2013 indicates that the product does not meet the standard of "Differential Pressu | Device recalls |
| Aug 1, 1994 | MAYTEX LATEX EXAMINATION GLOVES, POWDEREDK935314 · LYY | 510(k) clearances |
| Aug 1, 1994 | MAYTEX POWDER-FREE LATEX EXAMINATION GLOVESK935315 · LYY | 510(k) clearances |
| May 31, 1989 | MAYTEX LATEX EXAMINATION GLOVESK892183 · LYY | 510(k) clearances |
| May 31, 1989 | MAYTEX NON-STERILE LATEX EXAM GLOVESK892082 · LYY | 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
