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 R-Med, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 17, 2000: RIZA BAND STRETCHER (RBS)-60000.
| Jul 17, 2000 | RIZA BAND STRETCHER (RBS)-60000K001236 · FHN | 510(k) clearances |
| Jan 11, 1996 | R-MED ABDOMINAL WALL ELEVATORK953360 · HET | 510(k) clearances |
| Nov 16, 1995 | RIZA-RIBE NEEDLE (MODIFICATION)K954882 · HRX | 510(k) clearances |
| Aug 18, 1995 | RIZA-RIBE NEEDLEK953441 · FBK | 510(k) clearances |
| May 11, 1995 | R-MED MINI-RETRACTORK950108 · HET | 510(k) clearances |
| Mar 31, 1995 | R-MED DISPOSABLE PLUGK942411 · HET | 510(k) clearances |
| Dec 7, 1994 | R-MED MOTORIZED LAPAROSCOPIC HANDLEK945637 · GCJ | 510(k) clearances |
| Aug 29, 1994 | MANUAL LAPAROSOPIC HANDLE, INTERCHANGEABLE LAPAROSCOPIC TOOL UNITSK943818 · GEI | 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
