Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in JapanLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Medicon with 15 510(k) clearances. The most recent is a 510(k) clearance dated Feb 29, 2012: CLEANE / CLEANE POP.
| Date | Record | Source |
|---|---|---|
| Feb 29, 2012 | CLEANE / CLEANE POPK111341 · OZC | 510(k) clearances |
| Apr 23, 1997 | SERVOTRONIC EC100 SYSTEMK962087 · HWE | 510(k) clearances |
| Jun 22, 1995 | TITANIUM MANDIBULAR FRACTURE SYSTEMK952168 · JEY | 510(k) clearances |
| Jan 9, 1986 | TENS GB1001 DEVICEK850855 · GZJ | 510(k) clearances |
| Aug 21, 1985 | INFRARAX DEVICEK850852 · ILY | 510(k) clearances |
| Apr 1, 1985 | GAUZE ASORBABLEK844702 · EFQ | 510(k) clearances |
| Mar 5, 1985 | ABSORBABLE GAUZE PRODUCTSK844573 · EFQ | 510(k) clearances |
| Feb 21, 1985 | WHEELCHAIRSK844574 · IOR | 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
