# K113857: Synergetics Directional Endoocular Laser Probe

- Pathway: 510(k) (Traditional)
- Applicant: Synergetics, Inc.
- Decided: Apr 23, 2012 after 115 days
- Product code: HQB (Photocoagulator And Accessories)
- Device class: 2
- Regulation: 21 CFR 886.4690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K954307 (1995). 1 ancestor in all.
3 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954307: Gamp & Assoc. Disposable Endoocular Laser Probe, Gamp & Assoc. (1995) Summary page 1.

## Most influential descendants
- K142830: Ophthalmed Bending Laser Probes (2015), 2 descendants of its own
- K191846: MAXReach Laser Probe (2019), 1 descendant of its own
- K220263: Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical Chandeliers (2022), 0 descendants of its own

## Indications for use
The Synergetics Directional Endo Ocular Laser Probe provides a mean for delivering endophotocoagulation during vitrectomy surgery.

Source page: https://510kreport.com/device/K113857
Methodology: https://510kreport.com/methodology