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 Incutech, Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jun 20, 1996: MORE-L INJECTOR KIT PLUS.
| Date | Record | Source |
|---|---|---|
| Jun 20, 1996 | MORE-L INJECTOR KIT PLUSK960619 · CAZ | 510(k) clearances |
| Jan 22, 1996 | MORELL INJECTORK951870 · CAZ | 510(k) clearances |
| Jan 27, 1995 | SAFE VENT SYSTEMK942394 · FMF | 510(k) clearances |
| Jul 22, 1994 | EMPTY, SOLUTION TRANSFER CONTAINER WITH DETATCHABLE LEG SETK941731 · KPE | 510(k) clearances |
| Mar 28, 1994 | SOLUTION TRANSFER CONTAINER W/ATTACHED LEG SET (EMPTY)K940258 · KPE | 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
