Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Kermath Mfg. with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 12, 1987: T.O.P. 2000 (TOMOGRAPHIC ORIENTATED PLANNING).
| Date | Record | Source |
|---|---|---|
| May 12, 1987 | T.O.P. 2000 (TOMOGRAPHIC ORIENTATED PLANNING)K870221 · KPQ | 510(k) clearances |
| Nov 5, 1981 | KERMATH THERAPY SIMULATORK812726 · KPQ | 510(k) clearances |
| Sep 16, 1981 | KERMATH L/C ARMK812332 · KPR | 510(k) clearances |
| Jun 12, 1981 | KERMATH RADIOGRAPHIC HEAD STANDK811215 · KPR | 510(k) clearances |
| Aug 25, 1977 | VERSATOMEK771549 · IZF | 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
