Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FranceLabelled 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 15, 2026, FDA's public records list Institut Georges Lopez with 4 510(k) clearances and 1 device recall. The most recent is a 510(k) clearance dated Apr 25, 2025: DCX Disposable Cassette (DCX).
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.
| Apr 25, 2025 | DCX Disposable Cassette (DCX)K243998 · KDN | 510(k) clearances |
| Mar 13, 2025 | Brand Name: Celsior Cold Storage Solution Product Name: Celsior Cold Storage Solution Model/Catalog Number: 533682 Product Description: IClass II · The potential for risk of microbiological contamination of products due to inability to ensure sterility assurance throu | Device recalls |
| Jun 14, 2022 | PERF-GEN Pulsatile Perfusion SolutionK221386 · KDL | 510(k) clearances |
| Jun 14, 2022 | BEL-GEN Cold Storage SolutionK221387 · KDL | 510(k) clearances |
| Oct 15, 2021 | RM4 Control UnitK211224 · KDN | 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
