Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in South KoreaLabelled 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 13, 2026, FDA's public records list Daesung Maref Co., Ltd. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jul 19, 2023: LF900.
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 |
|---|---|---|
| Jul 19, 2023 | LF900K231437 · IRP | 510(k) clearances |
| Sep 1, 2021 | SP-1000, SP-2000K202395 · IRP | 510(k) clearances |
| Jul 2, 2021 | LX9maxK203498 · IRP | 510(k) clearances |
| Jun 22, 2021 | LF900K203019 · IRP | 510(k) clearances |
| Apr 22, 2021 | DVT-PROK203353 · JOW | 510(k) clearances |
| Mar 28, 2021 | DVT-4000SK203417 · JOW | 510(k) clearances |
| Dec 5, 2020 | DVT-2600K203016 · JOW | 510(k) clearances |
| Jan 11, 2017 | Lympha-Flow(LF1200)K160178 · IRP | 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
