# K010007: Adapt Laparoscopic Port & Adapt Reducer Cap

- Pathway: 510(k) (Traditional)
- Applicant: Taut, Inc.
- Decided: Feb 22, 2001 after 51 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
77 later devices descend from it; 8 cite it directly.
0 of 78 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
- K070158: R-Port Laparoscopic Access Device (2007), 69 descendants of its own
- K073170: R-Port II Laparoscopic Access Device (2007), 68 descendants of its own
- K082619: Sils Port, Models SILSPT5, SILSPT12 (2008), 58 descendants of its own
- K090902: Spider Single Port Surgical Device, Support Arm Accessory,  Model 90001, 90002, 90003 (2009), 46 descendants of its own
- K112208: Intutive Surgical DA Vinci Single Site Instruments and Accessories (2011), 43 descendants of its own

## Recalls of this device
- Mar 11, 2014 · Class II · Z-1326-2014: Complaints of leakage of insufflation gas through the device.
- Mar 11, 2014 · Class II · Z-1279-2014: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.
- Mar 11, 2014 · Class II · Z-1284-2014: Complaints were received of leakage of insufflation gas through the device, which can cause difficulty or delay in the completion of laparoscopic surgical procedures.

Source page: https://510kreport.com/device/K010007
Methodology: https://510kreport.com/methodology