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 14, 2026, FDA's public records list Poonglim Pharmatech, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 29, 2024: PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Lu….
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.
| May 29, 2024 | PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe; PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile SyringeK241190 · QNQ | 510(k) clearances |
| Sep 15, 2023 | PLPT LDV(Low Dead Volume) LC(Luer-Cone) Sterile Syringe, PLPT LDV(Low Dead Volume) LL(Luer-Lock) Sterile SyringeK221860 · QNQ | 510(k) clearances |
| Feb 16, 2021 | EZ-Injec LDV Sterile Safety NeedleK210444 · QNS | 510(k) clearances |
| Feb 16, 2021 | PLPT LDV (Low Dead Volume) Sterile SyringeK210443 · QNQ | 510(k) clearances |
| May 12, 2020 | EZ-Inject Single use NeedleK192222 · FMI | 510(k) clearances |
| Jun 21, 2018 | Kopac Sterile NeedleK172483 · FMI | 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
