# K001975: Ceralas D10 810NM Laser, Model Ceralas D10-60

- Pathway: 510(k) (Traditional)
- Applicant: Ceram Optec, Inc.
- Decided: Aug 4, 2000 after 36 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 3 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K082721: Laserpro 810, 940 and 980 Diode Laser Systems (2008), 7 descendants of its own
- K013201: Cardiofocus Diode Laser System, Models 60R, 60NR, 30NR (2002), 6 descendants of its own
- K040744: Atrilaze Soft Tissue Ablation System (2004), 5 descendants of its own
- K052495: Atrilaze Malleable Ablation Probe (2005), 4 descendants of its own
- K151890: Medical Diode Laser Systems (2015), 3 descendants of its own

Source page: https://510kreport.com/device/K001975
Methodology: https://510kreport.com/methodology