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 Inneuroco with 9 510(k) clearances. The most recent is a 510(k) clearance dated Sep 27, 2023: Thinline Sheath Introducer.
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.
| Sep 27, 2023 | Thinline Sheath IntroducerK232260 · DYB | 510(k) clearances |
| Jul 29, 2022 | 091 Balloon Guide CatheterK220331 · DQY | 510(k) clearances |
| Aug 2, 2019 | 046 Zenith FlexK190338 · NRY | 510(k) clearances |
| Oct 25, 2018 | 074 Zenith Flex SystemK181354 · NRY | 510(k) clearances |
| Apr 19, 2018 | Zenith Flex SystemK172167 · NRY | 510(k) clearances |
| Jan 26, 2018 | Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cmK173709 · DQY | 510(k) clearances |
| Dec 6, 2017 | 091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cmK172468 · DQY | 510(k) clearances |
| Oct 19, 2017 | 065 Zenith, 074 ZenithK171672 · DQY | 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
