# K915062: Dohlman Doane Keratoprothesis

- Pathway: 510(k) (Traditional)
- Applicant: Mackeen Consultants, Ltd.
- Decided: Jan 21, 1992 after 74 days
- Product code: HQM (Keratoprosthesis, Permanent Implant)
- Device class: 2
- Regulation: 21 CFR 886.3400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K121203: Boston Keratoprosthesis or Boston Kpro (2013), 1 descendant of its own
- K182986: Boston Keratoprosthesis, Type I Lucia (2019), 0 descendants of its own

Source page: https://510kreport.com/device/K915062
Methodology: https://510kreport.com/methodology