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 R.H. Burton Co. with 19 510(k) clearances. The most recent is a 510(k) clearance dated Jun 7, 1993: BURTON H- BASE TABLE - MODEL 1990.
| Jun 7, 1993 | BURTON H- BASE TABLE - MODEL 1990K924773 · HRX | 510(k) clearances |
| Apr 14, 1993 | BURTON TRIAL LENS SETK924786 · HPC | 510(k) clearances |
| Apr 14, 1993 | BURTON SLIT LAMP - MODEL 850K924783 · HJO | 510(k) clearances |
| Apr 14, 1993 | BURTON AUTOMATIC PROJECTOR - MODEL CP-40K924774 · HOD | 510(k) clearances |
| Apr 5, 1993 | BURTON LENSMETER - MODEL 2021K924776 · HLM | 510(k) clearances |
| Apr 5, 1993 | BURTON PROJECTOR HEAD - MODEL 6000-HK924784 · HOS | 510(k) clearances |
| Apr 5, 1993 | BURTON AUTO REFRACTOR/KERATOMETER - MODEL BARK-8K924778 · HKO | 510(k) clearances |
| Apr 5, 1993 | BURTON LENSMETERK924788 · HLM | 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
