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 Dmetec Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 27, 2017: COMPACT S, COMPACT S (LED).
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 |
|---|---|---|
| Dec 27, 2017 | COMPACT S, COMPACT S (LED)K170104 · ELC | 510(k) clearances |
| Dec 11, 2012 | ULTRASONIC SURGERYK121620 · DZI | 510(k) clearances |
| Jun 14, 2012 | ULTRASONIC SURGERY MACHINEK113152 · DZI | 510(k) clearances |
| Mar 29, 2006 | CLEANSE S+ ULTRASONIC SCALERK060171 · ELC | 510(k) clearances |
| Jul 19, 2005 | SKYLIGHT LED CURING LIGHTK051571 · EBZ | 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
