Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Enztec Limited with 5 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Sep 1, 2023: CONDUIT™ ATP Inserters.
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 1, 2023 | CONDUIT™ ATP InsertersK232014 · MAX | 510(k) clearances |
| Jun 27, 2023 | RI.KNEE Adjustable Tibia Cut GuideK230876 · OLO | 510(k) clearances |
| Jan 5, 2023 | CONDUIT LLIF Straight InsertersK223671 · MAX | 510(k) clearances |
| Jun 28, 2022 | DePuy CONDUIT LLIF SQUID InserterK220449 · MAX | 510(k) clearances |
| Nov 1, 2021 | DePuy CONDUIT LLIF Angled InsertersK212823 · MAX | 510(k) clearances |
| Aug 16, 2019 | REF 800-05-035, ENZTEC FEMORAL IMPACTOR - DJO, (01) 09421028110624 (10) 999999, To be used only with DJO EMPOWR 3D KNEEClass II · The femoral impactors have a higher than normal risk of the arm breaking. During impaction the tip of the arm may fractu | Device recalls |
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
