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Nuvis

INTEGRATED ENDOSCOPY, INC. · Model IE58CAN-2 · UDI-DI 00853816008018

NBH Prescription

510(k) clearances

5,174

Adverse events

Recalls

296

Facilities

Description

The cannula is a stainless-steel tube with no taper at the end, through which the Nuvis® arthroscope can be inserted into the body during arthroscopic surgery. It must be rigid and strong enough to protect the arthroscope from bending, breaking, chipping and any other potential damage that could befall the arthroscope during normal use. It will be able to accommodate the 4mm diameter of the arthroscope, while still leaving enough room for fluid movement. It must be an adequate length to protect the tip, but not long enough to block its image. This cannula version is named as dual rotating stopcock. This dual stopcock version is leak proof when used with an arthroscope, obturator, or trocar. The cannula locking mechanism is modeled after the Stryker SpeedLock™, so as to keep it similar to what the customer is used to. The cannula will be sold as a reusable non-sterile device and distributed independently. Each instrument is cleaned then sterilized by steam autoclave per customer policy and procedure.

Recalls

Date	Firm	Reason
2020-09-21	Smith & Nephew, Inc.	The J Lock feature on the cannula body was manufactured incorrectly, preventing the cannula from locking into an irrigation extender or arthroscope in the correct orientation.
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system
2019-06-25	BioPro, Inc.	Manufacturing flaw in the sterile barrier system

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.