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 13, 2026, FDA's public records list MTD, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 22, 2007: MEDICAL IMAGE MANAGEMENT DEVICES FOR VISION TOOLS.
| Date | Record | Source |
|---|---|---|
| Jan 22, 2007 | MEDICAL IMAGE MANAGEMENT DEVICES FOR VISION TOOLSK063439 · LLZ | 510(k) clearances |
| Jan 3, 1984 | ARMBOARDK833559 · KPR | 510(k) clearances |
| Sep 7, 1979 | THE MTD VARA SET CASETTE HOLDERK791374 · KPR | 510(k) clearances |
| Jan 3, 1978 | ARTHROSTRESSK772321 · JEB | 510(k) clearances |
| Sep 30, 1977 | PATIENT RESTRAINT SYSTEMK771659 · FMQ | 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
