# K001439: Orthoceph OC100 D

- Pathway: 510(k) (Traditional)
- Applicant: Instrumentarium Corp.
- Decided: Jun 22, 2000 after 45 days
- Product code: MUH (System, X-Ray, Extraoral Source, Digital)
- Device class: 2
- Regulation: 21 CFR 872.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
39 later devices descend from it; 4 cite it directly.
0 of 40 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
- K030699: Veraviewepocs Panoramic/Cephalometric X-Ray Unit with  Cephalometric (2003), 24 descendants of its own
- K073696: Veraviewepocs (2008), 22 descendants of its own
- K093683: Orthopantomograph OP300 (2010), 21 descendants of its own
- K111231: Panoura 18S (2011), 11 descendants of its own
- K043612: Orthopantomograph OP200, OP200D, and Orthoceph OC200, OC200D (2005), 10 descendants of its own

Source page: https://510kreport.com/device/K001439
Methodology: https://510kreport.com/methodology