# K945110: Kolberg Ophthalmic Conformer

- Pathway: 510(k) (Traditional)
- Applicant: Kolberg Ocular Products, Inc.
- Decided: Jan 13, 1995 after 87 days
- Product code: HQN (Conformer, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 886.3130
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K982562: Bio-Eye Hydroxyapatite Ocular Impland and Conformer (1998), 1 descendant of its own
- K021643: HA Orbital Implant (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K945110
Methodology: https://510kreport.com/methodology