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 13, 2026, FDA's public records list Bryan Corp. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Aug 10, 2000: BIOTRACE, MODEL 1730.
| Date | Record | Source |
|---|---|---|
| Aug 10, 2000 | BIOTRACE, MODEL 1730K002063 · MYU | 510(k) clearances |
| Sep 25, 1992 | MICROPROCESSED CONTROLLED LAPAROFLATORK913242 · HIF | 510(k) clearances |
| Oct 24, 1989 | DUMON TRACHEOBRONCHIAL STENTK894380 · NWA | 510(k) clearances |
| Jul 28, 1988 | BAGGISH, HYSTEROSCOPEK881249 · HIH | 510(k) clearances |
| Mar 12, 1986 | DUMON/HARRELLK854414 · EOQ | 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
