Brainlab AG
Brainlab AG holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2025, with 39 FDA device recalls on record.
Clearances by Brainlab AG — page 2
101–135 of 135- K042512 — VECTORVISION ACL
- K041703 — IPLAN!
- K042391 — KOLIBRI IMAGE GUIDED SURGERY SYSTEM
- K041899 — VECTORVISION UNI-KNEE
- K041330 — IPLAN! FLOW
- K040368 — VECTORVISION HIP 3.0
- K040931 — PATXFER RT
- K033316 — TABLE TILT DEVICE
- K040585 — EXACTRAC 4.0 AND EXACTRAC X-RAY 6D
- K023651 — VECTORVISION CRANIAL/ENT
- K032511 — INTUITION IMAGE
- K033287 — EXACTRAC GATING
- K031770 — CI TKR/UKR
- K024192 — VECTORVISION FLUORO3D
- K021306 — VECTORVISION CT-FREE KNEE
- K020631 — IPLAN
- K021583 — PATXFER
- K014256 — KOLIBRI IGS SYSTEMS
- K020860 — M3 (MICRO-MULTILEAF COLLIMATOR)
- K004022 — M3 (MIRCO-MULTILEAF COLLIMATOR
- K012448 — VECTORVISION TRAUMA
- K010602 — VECTORVISION HIP
- K010612 — VECTORVISION KNEE
- K012564 — MODIFICATION TO: VECTORVISION FRAMELESS BIOPSY SYSTEM
- K010968 — VECTORVISION CT/FLUORO
- K003285 — EXAC TRAC 2.0 (NOVALIS BODY MODULE)
- K003589 — VECTORVISION CRANIAL, VECTORVISION SPINAL, VECTORVISION ENT
- K003268 — Z-TOUCH
- K002509 — NOVALIS (SHAPED BEAM SURGERY SYSTEM)
- K994413 — BRAINSCAN
- K983410 — @ TARGET
- K983831 — VECTORVISION2
- K981508 — VECTORVISION SPINE MODULE
- K971367 — BRAINSCAN CONFORMAL RT MODULE
- K954789 — BRAINLAB HEADPINS
Data sourced from openFDA. This site is unofficial and independent of the FDA.