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 Ritmed, Inc. with 22 510(k) clearances. The most recent is a 510(k) clearance dated Feb 17, 1984: FLORET FOAM PREP SPONGE.
| Feb 17, 1984 | FLORET FOAM PREP SPONGEK833626 · GDY | 510(k) clearances |
| Sep 26, 1983 | ISOVIS WOUND PROTECTORK832874 · KKX | 510(k) clearances |
| Jun 24, 1983 | ISOVIS WOUND PROTECTORK830270 · KKX | 510(k) clearances |
| Jun 8, 1983 | FLORET CYLINDRICAL/BRONCHOSCOPIC/LAMINK830268 · EFQ | 510(k) clearances |
| Jun 8, 1983 | FLORET STRUNG GAUZE SPONGESK830261 · EFQ | 510(k) clearances |
| Jun 8, 1983 | FLORET KITTNER OR K DISSECTORK830266 · EFQ | 510(k) clearances |
| Jun 8, 1983 | FLORET SPECIAL GAUZE SPONGESK830267 · EFQ | 510(k) clearances |
| Jun 3, 1983 | PROTET HOLDERS-BLOCKS & ROLLK830272 · FWZ | 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
