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 Todd Medical, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Nov 27, 1987: CLOSED FOLEY CATHETER SYSTEM.
| Nov 27, 1987 | CLOSED FOLEY CATHETER SYSTEMK873288 · KNY | 510(k) clearances |
| Nov 24, 1987 | TODD MEDICAL/SKILLED CARE PRODUCTSK873499 · BTO | 510(k) clearances |
| Nov 13, 1987 | IRRIGATION TRAY (W/120CC OF STERILE NORMAL SALINE)K873287 · KOD | 510(k) clearances |
| Oct 29, 1987 | TODD MEDICAL/SKILLED CARE PRODUCTSK873469 · LRP | 510(k) clearances |
| Sep 3, 1985 | ECLIPSE SELF ADHERING ELECTRODEK850646 · GXY | 510(k) clearances |
| Apr 2, 1985 | TRANSCUTANEOUS NERVE STIMULATOR FOR PAIN RELIEFK850004 · GZJ | 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
