Direx Systems Corp.
Direx Systems Corp. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2012.
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.