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 Wonjin Mulsan with 5 510(k) clearances. The most recent is a 510(k) clearance dated Sep 14, 2021: Compressible Limb and Circulation Therapy System, Model POWER-Q2300.
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 14, 2021 | Compressible Limb and Circulation Therapy System, Model POWER-Q2300K211283 · IRP | 510(k) clearances |
| Mar 8, 2021 | Compressible Limb and Circulation Therapy SystemK200660 · IRP | 510(k) clearances |
| Feb 27, 2012 | COMPRESSIBLE LIMB THERAPY SYSTEMK113275 · IRP | 510(k) clearances |
| May 26, 2010 | COMPRESSIBLE LIMB THERAPY SYSTEM MODEL WHF-324 (POWER-Q1000 PLUS)K100656 · IRP | 510(k) clearances |
| Jan 23, 2009 | COMPRESSIBLE LIMB AND CIRCULATION THERAPY SYSTEM, MODEL WHF-314 (POWER-Q1000)K080134 · 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
