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 Slenderizers Equipment Manufacturing with 7 510(k) clearances. The most recent is a 510(k) clearance dated Jul 15, 1988: MULTI-FLEX TABLE--MODEL 200.
| Jul 15, 1988 | MULTI-FLEX TABLE--MODEL 200K881804 · JFB | 510(k) clearances |
| Jun 9, 1987 | MULTI-FLEX TABLE -- MODEL 105K870714 · JFB | 510(k) clearances |
| Jun 9, 1987 | MULTI-FLEX TABLE -- MODEL 101K870710 · JFB | 510(k) clearances |
| Jun 9, 1987 | MULTI-FLEX TABLE -- MODEL 102K870711 · JFB | 510(k) clearances |
| Jun 9, 1987 | MULTI-FLEX TABLE -- MODEL 103K870712 · JFB | 510(k) clearances |
| Jun 9, 1987 | MULTI-FLEX TABLE -- MODEL 104K870713 · JFB | 510(k) clearances |
| Jun 9, 1987 | MULTI-FLEX TABLE -- MODEL 106K870715 · JFB | 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
