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Retractor, Self-Retaining, For Neurosurgery

FDA product code GZT · Class 2 · Neurology

5,803
Registered devices
111
Adverse events
6
Recalls
43
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-06-19Nico Corp.Mislabeled hook pouch included a transport/storage label rather than the product label containing key product information such as part number, lot number, and
2012-08-21Vycor Medical, Inc.Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System) because an unidentified black fiber was found on the device.
2012-07-17Nico Corp.BrainPath sheaths were mislabeled. Sheaths which measure 50mm were labeled as 60mm. The length callout on the label does not match the actual length of the shea
2012-07-17Nico Corp.BrainPath sheaths were mislabeled. Sheaths which measure 50mm were labeled as 60mm. The length callout on the label does not match the actual length of the shea
2007-12-19Abbott SpineDislodged Collar Spring; The collar spring binding on the shaft of generic handle used with multiple surgical instruments has the potential to release the devic
2003-02-26Ohio Medical Instrument Co IncThe component was manufactured with an insufficient weld that could break during use.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.