Teleflex wins FDA nod for reusable surgical access systems

11/6/2012 | (Boston)

The FDA has given Teleflex 510(k) clearance to market its Weck obturators, which are used during minimally invasive procedures to give surgical tools access. The reusable devices work with Teleflex's Weck Vista single-use cannulas and with the firm's Weck Vista line of bladeless ports for laparoscopic access.

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