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 14, 2026, FDA's public records list Innobiosurg Co., Ltd. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Dec 20, 2022: IBS System.
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.
| Dec 20, 2022 | IBS SystemK220517 · DZE | 510(k) clearances |
| Dec 14, 2022 | Magicore Narrow SystemK220079 · DZE | 510(k) clearances |
| Oct 15, 2021 | Magicore SystemK212517 · DZE | 510(k) clearances |
| Aug 25, 2021 | Premilled Titanium Block SystemK203344 · NHA | 510(k) clearances |
| Dec 3, 2020 | Magic UCLA Abutment SystemK202418 · NHA | 510(k) clearances |
| Sep 23, 2020 | IBS Implant SystemK202479 · DZE | 510(k) clearances |
| Aug 27, 2020 | Magicore SystemK201981 · DZE | 510(k) clearances |
| Jul 15, 2020 | Magicore II SystemK201621 · NHA | 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
