Home › Device types › GZT
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
Black Belt Pronged Blade — KOROS U.S.A., INC.Multi Level BB Triple Blade Retractor — KOROS U.S.A., INC.V. Mueller — STERIS CORPORATIONBOSS Instruments — BOSS INSTRUMENTS, LTD., INC.BOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Stealth Surgical — BOSS INSTRUMENTS, LTD., INC.Stealth Surgical — BOSS INSTRUMENTS, LTD., INC.Two-sided angling blade holder for BluCLAS — Geister Medizintechnik GmbHAmbler Surgical — AMBLER SURGICAL CORP.Symmetry KARLIN™ — ASPEN SURGICAL PRODUCTS, INC.Black Belt II Tilting Arm Retractor Basic Set — KOROS U.S.A., INC.Black Belt Pronged Ti Blade — KOROS U.S.A., INC.Shim Holder — KOROS U.S.A., INC.BOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Avalign — Avalign Technologies, Inc.Retractor, Spinal, blade medial 70x24mm — Geister Medizintechnik GmbHNovo Surgical — NOVO SURGICAL, INC.BUDDE® — INTEGRA LIFESCIENCES CORPORATIONMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftVycor Viewsite Brain Access System with Alignment Clip — VYCOR MEDICAL, INC.Avalign — Avalign Technologies, Inc.Avalign — Avalign Technologies, Inc.Millennium — Avalign Technologies, Inc.Millennium — Avalign Technologies, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-06-19 | Nico 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 |
| 2012-08-21 | Vycor Medical, Inc. | Vycor Medical recalled their VBAS (Vycor Viewsite Brain Access System) because an unidentified black fiber was found on the device. |
| 2012-07-17 | Nico 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 |
| 2012-07-17 | Nico 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 |
| 2007-12-19 | Abbott Spine | Dislodged Collar Spring; The collar spring binding on the shaft of generic handle used with multiple surgical instruments has the potential to release the devic |
| 2003-02-26 | Ohio Medical Instrument Co Inc | The component was manufactured with an insufficient weld that could break during use. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
