FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list ZIIP, Inc. with 2 510(k) clearances and 1 warning letter. The most recent is a warning letter dated May 22, 2026: Warning letter: CAPA, Complaint handling, Design controls.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| May 22, 2026 | Warning letter: CAPA, Complaint handling, Design controlsCDRH | Warning letters |
| Sep 23, 2021 | ZIIP+ DeviceK212342 · NFO | 510(k) clearances |
| Feb 24, 2017 | ZIIP DeviceK161484 · NFO | 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
