# P990035: The Sunlight Omnisense (TM) Ultrasound Bone Sonometer

- Pathway: PMA
- Applicant: Beam-Med, Ltd.
- Decided: Jan 20, 2000 after 204 days
- Product code: MUA (Bone Sonometer)
- Device class: 2
- Regulation: 21 CFR 892.1180
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

## Most influential descendants
- K110646: Beammed Sunlight Miniomni Bone Sonometer (2011), 6 descendants of its own
- K180516: EchoS (2018), 2 descendants of its own
- K152020: Bindex BI-100 (2016), 2 descendants of its own
- K202514: EchoS Family (2021), 1 descendant of its own
- K161971: Bindex BI-2 (2017), 1 descendant of its own

Source page: https://510kreport.com/device/P990035
Methodology: https://510kreport.com/methodology