Medical device makerLabelled 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 15, 2026, FDA's public records list Meditech International with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 18, 2008: BIOFLEX LD-R100 TREATMENT HEAD.
| Dec 18, 2008 | BIOFLEX LD-R100 TREATMENT HEADK081355 · ILY | 510(k) clearances |
| Apr 2, 2008 | LD-I 75 AND LD-I 200K072551 · NHN | 510(k) clearances |
| Mar 13, 2006 | BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADSK051875 · ILY | 510(k) clearances |
| Feb 24, 2005 | BIOFLEX LD-175 AND LD-1200 TREATMENT HEADSK041885 · ILY | 510(k) clearances |
| Apr 10, 2003 | BIOFLEX PROFESSIONAL THERAPY SYSTEMK023621 · ILY | 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
