Direx Systems Corp.
FDA 510(k) medical device clearances.
Top product codes for Direx Systems Corp.
Recent clearances by Direx Systems Corp.
- K111947 — DUET MAGNA
- K102765 — PRONEX
- K072529 — TRACKPORT
- K071701 — TRACKLEAF-10
- K063482 — CROSSPLAN / ACCUSOFT-XL V.4.04
- K062147 — INTEGRA SL
- K062032 — ACCUSOFT, ACCUSOFT XL
- K061873 — VERT-X
- K061713 — MAGIS1;MAGIS2
- K052212 — MIGUE
- K053640 — INTEGRA
- K052705 — DART-12
- K043409 — ACCUCHANGER
- K050091 — TRIPTER-X1 COMPACT DUET SP (SEPARATED PULSE)
- K041213 — 3DSCOPE
- K041582 — MODIFICATION TO TRIPTER X-1 COMPACT DUET
- K040474 — ACCUSOFT
- K040470 — TRIPTER X-1 COMPACT
- K040553 — MODIFICATION TO ACCULEAF
- K032171 — ACCUSOFT
- K023535 — TRIPTER X-1 COMPACT DUET
- K021338 — ACCULEAF
Data sourced from openFDA. This site is unofficial and independent of the FDA.