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 14, 2026, FDA's public records list Lic-Orthion with 17 510(k) clearances. The most recent is a 510(k) clearance dated Apr 4, 1989: PATIENT EXAMINATION GLOVES (LATEX).
| Apr 4, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K891649 · LYY | 510(k) clearances |
| Jun 19, 1986 | LIC-ORTHION MULTI-THERAPY TREATMENT TABLEK862022 · JFB | 510(k) clearances |
| Feb 6, 1986 | DAISY (ABSORBENT INCONTINENCE SHIELD)K854730 · EYQ | 510(k) clearances |
| Feb 6, 1986 | ADAM (ABSORBENT INCONTINENCE SHIELD)K854729 · EYQ | 510(k) clearances |
| Jun 12, 1985 | TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTORK851471 · KNX | 510(k) clearances |
| Jun 12, 1985 | BIBAG, BIBAND & BIFIX - SINGLE USE URINE COLLECTORK851470 · KNX | 510(k) clearances |
| Oct 25, 1984 | CITOMAT AUTOCLAVESK843234 · ECG | 510(k) clearances |
| Oct 25, 1984 | ANATOM SYSTEMK843233 · KLC | 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
