# K924011: Origin Blunt Tip Surgical Trocar

- Pathway: 510(k) (Traditional)
- Applicant: Origin Medsystems, Inc.
- Decided: Jul 9, 1993 after 333 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: 7 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K060629: Gelport Blunt Tip Trocar System (2006), 4 descendants of its own
- K211577: SoftFix Balloon Trocar (2021), 2 descendants of its own
- K252714: C-Lant Port (2026), 0 descendants of its own
- K233263: Disposable Trocars (2024), 0 descendants of its own
- K191866: GelPOINT Mini Advanced Access Platform (2020), 0 descendants of its own

## Recalls of this device
- Feb 28, 2024 · Class II · Z-1470-2024: The potential for trocar seal disengagement when using mesh products incorrectly with the device.
- Feb 28, 2024 · Class II · Z-1469-2024: The potential for trocar seal disengagement when using mesh products incorrectly with the device.
- Feb 28, 2024 · Class II · Z-1465-2024: The potential for trocar seal disengagement when using mesh products incorrectly with the device.
- Feb 28, 2024 · Class II · Z-1468-2024: The potential for trocar seal disengagement when using mesh products incorrectly with the device.
- Feb 28, 2024 · Class II · Z-1471-2024: The potential for trocar seal disengagement when using mesh products incorrectly with the device.
- Feb 28, 2024 · Class II · Z-1466-2024: The potential for trocar seal disengagement when using mesh products incorrectly with the device.
- Feb 28, 2024 · Class II · Z-1467-2024: The potential for trocar seal disengagement when using mesh products incorrectly with the device.

Source page: https://510kreport.com/device/K924011
Methodology: https://510kreport.com/methodology