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 Jeneric Industries with 25 510(k) clearances. The most recent is a 510(k) clearance dated Sep 2, 1986: REXILLIUM N. B. F..
| Sep 2, 1986 | REXILLIUM N. B. F.K862822 · EJH | 510(k) clearances |
| Aug 29, 1986 | SURGICAL VITEXK862926 · ELE | 510(k) clearances |
| Jan 30, 1986 | H40 BASE METAL ALLOYK854878 · EJH | 510(k) clearances |
| Jan 9, 1985 | RX CBGK844122 · EJH | 510(k) clearances |
| Jan 9, 1985 | RX CBYK844123 · EJH | 510(k) clearances |
| May 1, 1984 | RX C & B 20K840563 · EJS | 510(k) clearances |
| May 1, 1984 | RX ELANK840561 · EJS | 510(k) clearances |
| Apr 13, 1984 | REX VK840562 · EJH | 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
