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 Radius International with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 23, 1998: RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT.
| Jan 23, 1998 | RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK972025 · KNT | 510(k) clearances |
| Jan 23, 1998 | RADIUS PUSH OVER THE GUIDE WIRE PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK972102 · KNT | 510(k) clearances |
| Jan 22, 1998 | RADIUS LOW PROFILE GASTROSTOMY TUBE KITK971901 · KNT | 510(k) clearances |
| Apr 17, 1995 | RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS)K951560 · IOR | 510(k) clearances |
| Feb 1, 1995 | RADIUS ENTERAL FEEDING TUBEK930510 · BSS | 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
