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 15, 2026, FDA's public records list Telemed Systems, Inc. with 22 510(k) clearances. The most recent is a 510(k) clearance dated May 6, 2002: PPD BALLOON DILATATION CATHETER.
| May 6, 2002 | PPD BALLOON DILATATION CATHETERK020379 · KNT | 510(k) clearances |
| Mar 1, 2002 | MODIFICATION TO: 3-LUMEN DURALON OCCLUSION BALLOONK013737 · FGE | 510(k) clearances |
| Apr 2, 2001 | FLEXIBLE ENDOSCOPIC SCISSORSK010412 · OCZ | 510(k) clearances |
| Dec 22, 1999 | 5.0 FRENCH X 200CM X 35MM TIP TAPER-20MM CUTTING WIRE, 5.0 FRENCH X 200CM X 35MM TIP TAPER-30MM CUTTING WIRE, 5.0 FRENCHK992402 · KNS | 510(k) clearances |
| Dec 22, 1999 | HOT BIOPSY FORCEPS FEENESTRATED 230 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATED 160 CM OVAL CUP, HOT BIOPSY FORCEPS SERRATDK992390 · KGE | 510(k) clearances |
| Jan 21, 1998 | REUSABLE BIOPSY FORCEPS OVAL CUP, REUSABLE BIOSY FORCEPS OVAL CUP W/NEEDLE, REUSABLE BIOPSY FORCEPS SERRATED CUP, REUSARK974312 · KNW | 510(k) clearances |
| Dec 19, 1997 | TELEMED SYSTEMS RETRIEVAL BASKETK974300 · OCZ | 510(k) clearances |
| Jul 16, 1990 | GASTROINTESTINAL CYTOLOGY BRUSHK901435 · FDX | 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
